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<|newrecord|> nctId: NCT06264076 id: 686340 id: CIV-NO-23-09-043976 type: OTHER domain: Eudamed CIV ID briefTitle: Ligament Balancing in Total Knee Arthroplasty acronym: BLIS-TKA overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2025-12-31 date: 2025-12-31 date: 2024-02-16 date: 2024-02-16 name: Oslo University Hos... |
1. Is it feasible to perform systematic ligament balancing on the MCL using a novel instrument? |
2. Can a novel instrument for ligament balancing acquire more objective and repeatable results, without risk of injury? |
Participants must consent prior to the surgery, but inclusion is only done once ligament balancing is indicated during surgery. Patients will be follow-up as standard protocol for Total Knee Arthroplasty patients at the hospital. conditions: Ligament; Laxity, Knee conditions: Knee Osteoarthritis studyType: INTERVENTION... |
<|newrecord|> nctId: NCT06264063 id: D-DIST briefTitle: Study of Behavioral Dysfunctions and Related Neuronal Correlates in Patients With Dystonia acronym: D-DIST overallStatus: RECRUITING date: 2024-01-10 date: 2024-03-10 date: 2025-10-10 date: 2024-02-16 date: 2024-02-16 name: IRCCS Centro Neurolesi "Bonino-Pulejo" c... |
Based on these premises, the present project aims to evaluate the cognitive and affective aspects of dystonias, in line with neuroimaging research documenting structural and functional dysfunctions in the respective brain regions. conditions: Dystonia conditions: Neurologic Disorder conditions: NEUROSCIENCE studyType: ... |
<|newrecord|> nctId: NCT06264050 id: 2023.04 briefTitle: Psychological Support Group and Its Effects on Mood, Anxiety and Coping acronym: SUPPORT overallStatus: ACTIVE_NOT_RECRUITING date: 2004-01-08 date: 2024-09-08 date: 2025-03-15 date: 2024-02-16 date: 2024-02-16 name: IRCCS San Camillo, Venezia, Italy class: OTHER... |
It is therefore an observational study with a pre-post design on a cohort of patients hospitalized at San Camillo IRCCS who attend the Psychological Support Group. |
The study consists of verifying whether the therapeutic activity of the Psychological Support Group (GSP) has an influence on the levels of anxiety, mood and coping skills in the patients who attend it. These purposes will be pursued through the administration to each patient at the beginning (pre) and at the end (post... |
<|newrecord|> nctId: NCT06264037 id: 2023.03 id: Studio 1574 /IRCCS San Camillo type: OTHER domain: CESC di Venezia e IRCSS San Camillo briefTitle: The Experience in Neurorehabilitation Setting: a Qualitative Study acronym: NURSEXPERIENCE overallStatus: RECRUITING date: 2023-03-15 date: 2024-12-08 date: 2025-03-15 date... |
<|newrecord|> nctId: NCT06264024 id: 519516 briefTitle: Simultaneous pHototherapeutic Keratectomy and corneAl Collagen cRosslinking in Eyes With Keratoconus: a Randomized Trial (SHARK) overallStatus: RECRUITING date: 2024-02-12 date: 2025-05-01 date: 2034-02-01 date: 2024-02-16 date: 2024-02-16 name: Oslo University Ho... |
The main questions it aims to answer are whether combined treatment can give better visual acuity and if the treatments are equally safe. conditions: Keratoconus studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: NONE count: 81 type: ESTIMATED name... |
<|newrecord|> nctId: NCT06264011 id: 2023B0044 briefTitle: Discrimination and Religious Experiences of Adult Muslimahs in Salaat acronym: DREAMS overallStatus: RECRUITING date: 2023-07-13 date: 2024-06 date: 2024-06 date: 2024-02-16 date: 2024-04-26 name: Ohio State University class: OTHER briefSummary: This goal of th... |
Participants will complete 15 questionnaires. Participants will be connected to a Heart Rate Variability (HRV) monitor as well as a 32-electrode EEG cap. After the baseline data are obtained, all participants will complete both conditions (salaat and counting) but the order of participation in conditions will be random... |
All participants will pray the Duha prayer, an optional superogatory prayer that typically occurs in the early morning, to control for differences in timing and duration of prayer. The Duha is completed between the dawn and noon prayers and consists of four cycles of prayer as well as Qur'an recitation and supplication... |
<|newrecord|> nctId: NCT06263998 id: HUC1-394 briefTitle: Clinical Study for the Evaluation of Safety and Tolerability of NCP112 Eye Drops overallStatus: NOT_YET_RECRUITING date: 2024-06-03 date: 2025-11-28 date: 2026-01-30 date: 2024-02-16 date: 2024-02-16 name: Huons Co., Ltd. class: INDUSTRY briefSummary: The object... |
<|newrecord|> nctId: NCT06263985 id: 20214133 briefTitle: Axis(TM) Solvent-dehydrate Dermal Allograft in the Treatment of Pelvic Organ Prolapse. overallStatus: ACTIVE_NOT_RECRUITING date: 2021-11-02 date: 2025-05-30 date: 2025-05-30 date: 2024-02-16 date: 2024-02-16 name: Michigan Institution of Women's Health PC class... |
* Is the leading edge of the prolapse above the hymen |
* Does subject notice a bulge Participants will undergo Axis Dermis pelvic organ prolapse repair procedure. conditions: Pelvic Organ Prolapse studyType: INTERVENTIONAL phases: PHASE4 allocation: NA interventionModel: SINGLE_GROUP interventionModelDescription: Subjects undergoing the treatment for pelvic organ prolapse ... |
<|newrecord|> nctId: NCT06263972 id: 0168-21EMC briefTitle: Comparison of the Efficacy of Transcranial Direct Current Stimulation (tDCS) of the Primary Motor Cortex (M1) or the Prefrontal Cortex Combined With Aerobic Activity for Alleviation of Fibromyalgia Symptoms. overallStatus: NOT_YET_RECRUITING date: 2024-03 date... |
Participants will be randomly assigned to stimulation in a ratio of 1:1:1. 120 participants (40 in each group). The therapeutic course will include moderate aerobic physical activity (at 60% of the target heart rate adjusted for age) 3 times a week for 4 weeks (a week of adjustment, and 3 weeks of treatment), along wit... |
<|newrecord|> nctId: NCT06263959 id: GST-HG131-II-01 briefTitle: A Randomized, Double-blind, Placebo-controlled Phase IIa Clinical Study to Evaluate the Safety and Efficacy of GST-HG131 Tablets in Patients With Chronic Hepatitis B overallStatus: RECRUITING date: 2023-12-29 date: 2024-09-01 date: 2024-11-01 date: 2024-0... |
<|newrecord|> nctId: NCT06263946 id: WS10337 briefTitle: Essilor® Stellest® Lenses Multicentre European Study (SLOMES) acronym: SLOMES overallStatus: RECRUITING date: 2024-03-22 date: 2026-09-30 date: 2026-12-30 date: 2024-02-16 date: 2024-04-03 name: Essilor International class: INDUSTRY briefSummary: The goal of this... |
<|newrecord|> nctId: NCT06263933 id: 2023-A01804-41 briefTitle: Effect of Experience Sharing and Mutual Assistance on Insight and Recovery During the First Psychotic Episode acronym: DIPEM overallStatus: RECRUITING date: 2023-11-13 date: 2024-11-13 date: 2025-11-13 date: 2024-02-16 date: 2024-02-16 name: Centre hospita... |
<|newrecord|> nctId: NCT06263920 id: 288703 briefTitle: Neurofrailty: A Study of Late-onset Epilepsy and Its Associations overallStatus: RECRUITING date: 2022-05-05 date: 2027-01-12 date: 2027-01-12 date: 2024-02-16 date: 2024-02-16 name: Lancashire Teaching Hospitals NHS Foundation Trust class: OTHER briefSummary: We ... |
The NeuroFrailty study involves observing people from the time of diagnosis of first seizure. At this time, we will look at investigations such as blood tests, blood pressure, brain scans, alongside other diagnoses which might tell us whether there are differences compared to people without seizures. For some people, w... |
Over the following years, we will look at how things change: for example whether there are changes in memory, new diagnoses, medication changes and how lifestyle has changed. Because there is so little research in this area, it is very difficult to predict what might happen. For example, some people can experience wors... |
Purpose and Background |
Most of the time, we do not know why an adult develops epilepsy. Some researchers think there may be a connection between epilepsy which starts in adulthood, and increased risk of stroke or dementia in the future. However, there is very little research or evidence in this area, so we cannot say whether this is true. |
What does taking part involve? |
This study is an observational study, which means that the management of participants' seizure disorder will not be affected if they choose to take part in this study. The purpose of this study is to watch participants over the course of several years, to find out more about seizures which start in adulthood. |
Participants can choose the level of involvement that is right for them. |
1. LOW involvement. A researcher will check hospital and General Practice (GP records) once or twice per year, for the LIMITED AND SPECIFIC purpose of checking: medications, any new diagnoses, investigations associated with stroke risk (such as cholesterol, blood pressure, heart trace) and any brain scans that have bee... |
2. HIGH involvement. This involves being contacted by telephone once per year for 15-30 minutes to ask questions assessing memory and enquiring about lifestyle, such as exercise, smoking and alcohol use. |
3. VERY HIGH involvement. These participants will be contacted for a longer telephone conversation 30-45 minutes once per year about their experience of how epilepsy has affected home life, work and medications. |
If someone decides in the future that they don't want to be involved, they can withdraw from the study. However, once the study is completely finished, the information will be completely anonymous, which means that I won't be able to find individual's information in order to delete it. |
Glossary Seizure disorder = any disorder which involved having experienced at least one seizure. First seizure and epilepsy both can be classed as a form of seizure disorder. |
Neurofrailty = A condition whereby a person is at risk of stroke or dementia. conditions: Late Onset Epilepsy conditions: Stroke conditions: Dementia studyType: OBSERVATIONAL observationalModel: CASE_CONTROL timePerspective: PROSPECTIVE count: 360 type: ESTIMATED measure: At the time of onset, do people with late-onset... |
<|newrecord|> nctId: NCT06263907 id: stellate ganglion block briefTitle: Stellate Ganglion Block for Prevention of Post Mastectomy Depression acronym: SGB overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2024-12-31 date: 2025-04-30 date: 2024-02-16 date: 2024-02-28 name: Mansoura University class: OTHER briefSu... |
<|newrecord|> nctId: NCT06263894 id: MarmaraU-Ebe-ZDY-01 briefTitle: Alexander Technique on Labor Pain and Anxiety overallStatus: RECRUITING date: 2024-02-05 date: 2024-06-01 date: 2024-07-02 date: 2024-02-16 date: 2024-02-20 name: Marmara University class: OTHER name: The Scientific and Technological Research Council ... |
<|newrecord|> nctId: NCT06263881 id: MMH-407-009 briefTitle: Clinical Trial of the Efficacy and Safety of Raphamin in Combined Treatment of Community-acquired Pneumonia overallStatus: RECRUITING date: 2023-12-01 date: 2026-12-31 date: 2026-12-31 date: 2024-02-16 date: 2024-04-19 name: Materia Medica Holding class: INDU... |
<|newrecord|> nctId: NCT06263868 id: 69HCL23_1090 id: 2023-A02313-42 type: OTHER domain: ID-RCB briefTitle: First Observatory of Precocious Puberty. acronym: PAPPEL overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2028-03-01 date: 2028-03-01 date: 2024-02-16 date: 2024-02-20 name: Hospices Civils de Lyon class:... |
Due to a lack of studies and additional data, the reasons for this development are difficult to understand. Among current hypotheses, the entanglement with the evolution of our environment is at the forefront: the action of environmental endocrine disruptors and nutritional factors could play a role in the process of e... |
The establishment of a national observatory for early and advanced puberty in collaboration with pediatric endocrinologists (on the front line) would allow a reliable and precise field approach, capable of supplementing epidemiological data, which are currently insufficient. |
The investigators hypothesize that the establishment of an observatory of pubertal advances (early puberty and advanced puberty) in private medicine is possible, with inclusion of at least 75% of eligible patients, and collection of at least 80% of data. conditions: Puberty, Precocious studyType: OBSERVATIONAL observat... |
<|newrecord|> nctId: NCT06263855 id: 24-000352 briefTitle: Effect of Large Language Model in Assisting Discharge Summary Notes Writing for Hospitalized Patients overallStatus: ENROLLING_BY_INVITATION date: 2024-07-01 date: 2024-12-31 date: 2025-04-01 date: 2024-02-16 date: 2024-04-05 name: Mayo Clinic class: OTHER brie... |
<|newrecord|> nctId: NCT06263842 id: KFSIRB200-132 briefTitle: Elamrousy Novel Approach of Socket Shield Technique overallStatus: RECRUITING date: 2024-02-10 date: 2025-02-10 date: 2025-02-20 date: 2024-02-16 date: 2024-03-12 name: Kafrelsheikh University class: OTHER briefSummary: The current trial aim was to evaluate... |
The present study included 63 patients, aged 20 to 45, with teeth that needed to be extracted. After Kafrelsheikh University research ethics committee approval, patients were randomized into 3 groups: group I patients underwent immediate implantation using socket shield protocol, while group II patients underwent the s... |
<|newrecord|> nctId: NCT06263829 id: 2023-1580 briefTitle: HCV Tappt Adherence Study overallStatus: NOT_YET_RECRUITING date: 2024-07-01 date: 2025-01-01 date: 2025-07-01 date: 2024-02-16 date: 2024-02-16 name: University of Illinois at Chicago class: OTHER name: Synchronyx name: American Society of Health-System Pharma... |
* The primary aim is to assess the non-inferiority of Tappt with medication adherence, treatment completion, sustained virologic response (SVR) assessment, and SVR achievement rates. |
* The secondary aim is to assess the efficacy of Tappt at enabling pharmacists to personalize treatment and management decision based on participants' reported barriers to adherence, care, and SVR achievement. |
Participants will download and utilize the Tappt app to record adherence to oral medication. For the purposes of this study, adherence for participants in the intervention arm will be measured using a modified medication possession ratio (MPR) measure called medication tag scan ratio (MTSR). MTSR is defined as a percen... |
Upon study completion, a retrospective matched control will be established for the intervention group. Historic data for the matched control's adherence, treatment completion, SVR assessment, and SVR rates will be compared to the intervention arm. conditions: Hepatitis C studyType: INTERVENTIONAL phases: NA allocation:... |
<|newrecord|> nctId: NCT06263816 id: CARVECIR briefTitle: Effect of Long-term Carvedilol to Prevent Decompensation or Death in Patients With Asymptomatic Child-Pugh A5 to B8 Cirrhosis and Clinically Significant Portal Hypertension: a Multicenter Double-blind Randomized Control Trial acronym: CARVECIR overallStatus: NOT... |
The usefulness of carvedilol to prevent decompensation of cirrhosis in patients with TE-LSM ≥ 25 kPa as a surrogate marker for clinically significant portal hypertension, has never been evaluated in a clinical trial. conditions: Asymptomatic Cirrhosis conditions: Clinically Significant Portal Hypertension studyType: IN... |
<|newrecord|> nctId: NCT06263803 id: Karataymusic briefTitle: The Effect of Listening to Music on Chronic Low Back Pain overallStatus: RECRUITING date: 2024-02-01 date: 2024-04-01 date: 2024-04-15 date: 2024-02-16 date: 2024-02-16 name: KTO Karatay University class: OTHER briefSummary: The effects of passive music list... |
<|newrecord|> nctId: NCT06263790 id: NEOUNIPD1(2024) briefTitle: Intubating Laryngeal Mask vs Direct Laryngoscopy: a Crossover Randomized Controlled Preterm Manikin Trial overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2024-03 date: 2024-03 date: 2024-02-16 date: 2024-02-16 name: University Hospital Padova class:... |
This is an unblinded, randomized, controlled, crossover (AB/BA) pilot trial of intubation procedure through intubating laryngeal mask vs direct laryngoscopy in a manikin simulating a term newborn. conditions: Neonatal Disease conditions: Intubation; Difficult or Failed studyType: INTERVENTIONAL phases: NA allocation: R... |
<|newrecord|> nctId: NCT06263777 id: P.T.REC/012/004142 briefTitle: Early Detection of Children With Developmental Disabilities in Assiut Governorate overallStatus: COMPLETED date: 2021-01-01 date: 2021-03-15 date: 2021-09-30 date: 2024-02-16 date: 2024-02-16 name: Beni-Suef University class: OTHER briefSummary: The st... |
<|newrecord|> nctId: NCT06263764 id: 23-11-1954 briefTitle: The Effect of Listening to Qur'an Recital on Quality of Life in Systemic Lupus Erythematosus Patients overallStatus: RECRUITING date: 2024-02-12 date: 2024-06-30 date: 2024-07-31 date: 2024-02-16 date: 2024-02-16 name: Indonesia University class: OTHER briefSu... |
<|newrecord|> nctId: NCT06263751 id: 202401096 id: 24FIM1268045 type: OTHER_GRANT domain: American Heart Association briefTitle: Comparing the Effectiveness of Two Produce Prescription Approaches On Fruit and Vegetable Intake and Food Security, While Exploring Implementation Outcomes Such as Reach, Implementation, Sust... |
<|newrecord|> nctId: NCT06263738 id: 2024-248 briefTitle: Cold and Heat Investigation to Lower Levels of Depression acronym: CHILL'D overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2027-04-01 date: 2027-04-01 date: 2024-02-16 date: 2024-03-28 name: Vail Health Behavioral Health class: OTHER name: Steadman Phil... |
<|newrecord|> nctId: NCT06263725 id: ALyster briefTitle: Protein Restriction (PR) for Weight Loss acronym: PR overallStatus: COMPLETED date: 2021-10-01 date: 2023-12-31 date: 2023-12-31 date: 2024-02-16 date: 2024-02-16 name: University of Copenhagen class: OTHER briefSummary: Prolonged dietary protein restriction has ... |
<|newrecord|> nctId: NCT06263712 id: 2021-02504 (Project 2) briefTitle: Differences Between Suicide Attempters and Suicide Ideators. Influence of the Brief Therapy Attempted Suicide Short Intervention Program (ASSIP) on Neuropsychological Correlates and Psychological Process Factors - Project 2 acronym: NePsyAssip HT o... |
The overall aim of project 2 is to investigate how the (neuro-) psychological patterns are modulated by the Attempted Suicide Short Intervention Program (ASSIP). Therefore, suicide attempters participating in this project 2 will be randomly assigned to either the intervention group ASSIP or a standard care plus resourc... |
At the end of the assessment in project 1 participants who reported a history of past suicide attempt (SUAT) will be informed about project 2. |
Only if participants agreed to take part in project 2 and have signed the informed consent, they are randomized into two conditions: The ASSIP intervention (ASSIP) versus standard of care plus resource interview (STAR). Participants of both groups will be assessed again 4 weeks and 12 months after their first baseline ... |
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