Clinical trials: Follow-up
Severe Neurological Disabilities
Medico-economic Impact Evaluation in Telemedecine Follow-up in Complement of a Mobile Team in Patients With Neurological Disabilities (HANDI@CCESS)
Access to care for people with traumatic or degenerative neurological disabilities is a current public health concern. New technological tools such as telemedicine can bring expertise to the place of life of people while…
- Trial name
- HANDI@CCESS (NCT03717974)
- Testing
- Telemedecine follow-up after an intervention at home of the mobile team, Mobile team follow-up after an intervention at home of the mobile team
- Where
- France
- Volunteers
- 80 people
- Sponsor
- Pôle Saint Hélier
Stroke
Structured Post-stroke Follow-up in Malmö, Sweden (SUESIM)
Background Stroke-related medical complications and health problems are common among stroke survivors. Post-stroke Checklist (PSC), developed by an international expert group, and can be used as a clinical tool to identify common…
- Trial name
- SUESIM (NCT04295226)
- Testing
- Structured follow-up after stroke.
- Where
- Sweden
- Volunteers
- 200 people
- Sponsor
- Region Skane
Diabete Type 2
Assessment of Personalized Follow-up in Prevention of Type 2 Diabetes
In France, the overall prevalence of diabetes was estimated at 5% of population in 2016, type 2 diabetes (T2DM) corresponding to 90% of cases.
- Trial name
- Proxipart (NCT05325710)
- Testing
- Study nurse intervention
- Where
- France
- Volunteers
- 230 people
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche
Type 2 Diabetes Mellitus (T2DM), Hyperglycemia
Effects of Short and Long Courses of Intermittent Hypoxic-Hyperoxic Training in Patients With Type 2 Diabetes Including Elderly
This is a single-center randomized controlled trial evaluating the efficacy and safety of short (3 days) versus long (10 days) courses of intermittent hypoxic-hyperoxic training (IHHT) in patients with type 2 diabetes mellitus…
- Conditions
- Type 2 Diabetes Mellitus (T2DM), Hyperglycemia, Metabolic Syndrome, Older Adults (65 Years and Older)
- Trial name
- EFIR (NCT07574333)
- Testing
- Intermittent Hypoxic-Hyperoxic Training (3 days), Intermittent Hypoxic-Hyperoxic Training (10 days), Normoxic gas breathing
- Where
- Russia
- Volunteers
- 250 people
- Sponsor
- National Medical Research Center for Therapy and Preventive Medicine
Myopia, Progressive
Slow Myopia Progression With Different Irradiance Light
It is a prospective clinical control study on red light control myopia with specail design spectacles for 75 children in 3 groups. Study Groups with two different powers of 0.6 mW and 1.2 mW at wavelength of 650nm.
- Trial name
- NCT05881655
- Testing
- Airdoc Red Lighting Device, Special Spectacles to Control Myopia
- Where
- China
- Volunteers
- 75 people
- Sponsor
- Beijing Airdoc Technology Co., Ltd.
Cervical Degenerative Disc Disorder
Post-Approval Study Protocol for the Simplify Cervical Artificial Disc
This study is intended to demonstrate the 5-year long-term safety and efficacy of the Simplify® Cervical Artificial Disc ("Simplify Disc") in subjects enrolled in the non-randomized Simplify Disc IDE study.
- Trial name
- NCT04630626
- Testing
- Simplify Disc, ACDF
- Where
- 15 sites in United States
- Volunteers
- 145 people
- Sponsor
- NuVasive
Childhood Cancer, Survivorship
Aftercare of Childhood Cancer Survivors in Switzerland
The Aftercare of Childhood Cancer Survivors in Switzerland (ACCS) study is a multicenter cohort study designed to investigate transition of follow-up care from pediatric oncology to adult care in a prospective and longitudinal…
- Conditions
- Childhood Cancer, Survivorship, Transition
- Trial name
- ACCS (NCT04284189)
- Testing
- Transition model
- Where
- 3 sites in Switzerland
- Volunteers
- 140 people
- Sponsor
- Kantonsspital Aarau
Prospective Studies, Heart Failure
Correlation Between Peripheral Venous Pressure and Central Venous Pressure in the Cardiac Intensive Care Unit
In patients admitted to a coronary care unit, what is the correlation coefficient and limits of agreement for paired measurements of peripheral venous pressure and central venous pressure at multiple time points during the…
- Trial name
- NCT03526497
- Where
- United States
- Volunteers
- 9 people
- Sponsor
- The Cleveland Clinic
Very Low Birth Weight Infant, Very Preterm Maturity of Infant
Swiss Neonatal Network & Follow-up Group
The chief aim of the Swiss Neonatal Network \& Follow-Up Group (SwissNeoNet) is to maintain and / or improve the quality and safety of medical care for high-risk newborn infants and their families in Switzerland through a…
- Conditions
- Very Low Birth Weight Infant, Very Preterm Maturity of Infant, Asphyxia Neonatorum
- Trial name
- SwissNeoNet (NCT04239508)
- Where
- Switzerland
- Volunteers
- 1,000 people
- Sponsor
- Swiss Neonatal Network
Arrythmia
Patient Specific Optimized Therapy Post-Market Clinical Follow-up Study
Study to evaluate the safety and procedural performance of the KODEX - EPD System when used in the treatment of cardiac arrhythmias.
- Trial name
- PSOT-PMCF (NCT03481413)
- Testing
- Ablation
- Where
- 22 sites in United States, Belgium and 6 more
- Volunteers
- 566 people
- Sponsor
- EPD Solutions, A Philips Company
Severe and Symptomatic Aortic Stenosis
Long-term Clinical and Echographic Follow-up (More Than 4 Years) After TAVI.
Transcatheter Aortic Valve Implantation (TAVI) is became the gold-standard therapy for patients with severe and symptomatic aortic stenosis with high operative risk or not suitable for surgery.
- Trial name
- NCT03402724
- Testing
- echographic
- Where
- France
- Volunteers
- 178 people
- Sponsor
- University Hospital, Montpellier
Critically Ill, Acute Kidney Injury
Non-interventional Follow-up Versus Fluid Bolus in RESPONSE to Oliguria in the Critically Ill
Background: After hypotension, oliguria (urine output less than 0.5 mL/kg/h) was the most common trigger to administer fluid bolus in a multinational practice survey in intensive care.
- Conditions
- Critically Ill, Acute Kidney Injury, Sepsis, Oliguria
- Trial name
- RESPONSE (NCT02860572)
- Testing
- follow-up without intervention, fluid bolus
- Where
- 2 sites in Finland
- Volunteers
- 130 people
- Sponsor
- Helsinki University Central Hospital
Heart Failure
HeartLogic™ in Patients With Heart Failure.
This randomized, multicenter clinical trial will evaluate whether remote management guided by the HeartLogic™ algorithm improves outcomes compared with traditional face-to-face follow-up in adult patients with heart failure…
- Trial name
- HERO (NCT07544771)
- Testing
- Alert-guided remote follow-up, Traditional follow up
- Where
- 15 sites in France
- Volunteers
- 578 people
- Sponsor
- Poitiers University Hospital
Neurodevelopmental Abnormality
Long-term Neurodevelopmental Disorders of Prematurely Born Children and Parental Experience
Thanks to the evolution in knowledge and technical advances in premature newborn intensive care, the survival of very premature infants is now possible. However, prognosis remain sometimes uncertain.
- Trial name
- PREMA7 (NCT04607109)
- Where
- France
- Volunteers
- 238 people
- Sponsor
- Central Hospital, Nancy, France
Maternal Health, Pregnancy Complications
Wakobo-ti-Kodro: Improving Identification of Pregnancy at Risk of Obstetric Complications at Community Level
This project aims to improve maternal health indicators in a national context where the maternal mortality rate is one of the highest in the world.
- Trial name
- NCT06613867
- Testing
- Wakobotikodro
- Where
- Central African Republic
- Volunteers
- 1,857 people, healthy volunteers welcome
- Sponsor
- Alliance for International Medical Action
TMJ Disc Disorder, TMJ Pain
MDR-JuggerKnot Mini Soft Anchor in Maxillofacial TMJ
The objective of this retrospective consecutive series PMCF study is to collect data confirming safety, performance and clinical benefits of the JuggerKnot Mini Soft Anchor (implant and instrumentation) when used for soft tissue…
- Conditions
- TMJ Disc Disorder, TMJ Pain, TMJ Sounds on Opening/Closing the Jaw, TMJ Disease
- Trial name
- NCT04033692
- Testing
- JuggerKnot Mini Soft Anchor
- Volunteers
- healthy volunteers welcome
- Sponsor
- Zimmer Biomet
Repair of Dura Mater
Clinical Investigation Plan - Post-market Clinical Follow-up Study Collagen Dura Membrane - Suturable
Monitoring the use of Collagen Dura Membrane - Suturable (DMS) in the post-market phase
- Trial name
- NCT07217132
- Testing
- Post-market Study
- Where
- United States
- Volunteers
- 54 people
- Sponsor
- Collagen Matrix
Sportsman's Groin Hernia
The Management of Sportsman's Groin Hernia in Professional and Amateur Soccer Players
The purpose of this study is to compare the surgical treatment for sportsman's hernia in our department to the current literature.
- Trial name
- NCT01752387
- Volunteers
- 246 people, healthy volunteers welcome
- Sponsor
- HaEmek Medical Center, Israel
Breast Cancer
Breast Imaging Studies in Women at High Genetic Risk of Breast Cancer: Annual Follow-Up Study
This study will explore new screening methods for early detection of breast and ovarian cancer in women at high risk for these diseases, because they have an altered breast cancer 1 (BRCA1) or breast cancer 2 (BRCA2) gene.
- Trial name
- NCT00006421
- Testing
- 2-Fluorodeoxyglucose
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- National Cancer Institute (NCI)
Pelvic Organ Prolapse
Anterior Prolapse Repair With and Without Graft Augmentation
This is a randomized control trial comparing anterior colporrhaphy with augmentation with dermal allograft (ARCUS) to anterior colporrhaphy with a suture-based repair (native tissue).
- Trial name
- ARCUS (NCT04085952)
- Testing
- dermal graft (ARCUS repliform) for anterior colporrhaphy, suture based anterior colporrhaphy
- Volunteers
- 114 people, healthy volunteers welcome
- Sponsor
- Endeavor Health
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