Clinical trials
Registry clinical trials
Below are recruiting registry clinical trials, each written for real people, not researchers. We’re tracking 1,406 recruiting studies, each written for real people, not researchers, below.
Recruiting studies
- NCT06606756Recruiting
Registry for children with inflammatory bowel disease
This registry collects information about children and teenagers with inflammatory bowel disease (IBD) to help doctors better understand and treat the condition. By joining, you'll help researchers learn more about IBD in young people.
GiessenAges Up to 18 years - NCT07196930Recruiting
Valvular heart disease in women registry
This study is a registry that collects data on women with valvular heart disease (heart valve problems). It aims to better understand how these conditions affect women and improve their care. You may join if you have a heart valve condition and are treated at a participating center.
AswānAges 18 years+ - NCT00404989Recruiting
Pregnancy drug safety registry for people with HIV treatment
This trial is a pregnancy registry that collects information about birth outcomes when certain HIV medicines are taken during pregnancy. It helps detect any major birth defects so future pregnancies can be safer.
Wilmington, North CarolinaAges 12–60 - NCT04504955Recruiting
Atopic dermatitis patient registry for medication safety and results
This study is a real-world registry that collects information from adults with atopic dermatitis (eczema) to track how newly started treatments work and how safe they are over time. It may help researchers and doctors better understand medication effects in everyday care.
Waltham, MassachusettsAges 18 years+ - NCT07598058Recruiting
Hand Eczema Treatment Safety and Effectiveness Registry
This registry collects information about how well medications work for chronic hand eczema and how safe they are over time. You'll share your health data and treatment experiences through simple online forms to help doctors better understand which treatments work best.
Waltham, MassachusettsAges 18 years+ - NCT04292574Recruiting
UK Spinal Muscular Atrophy patient registry
This trial is a registry that collects health information from people with spinal muscular atrophy (SMA). It helps researchers understand the condition better and may support future studies and treatments.
Newcastle upon TyneAges Any age - NCT07256249Recruiting
Registry studying a drug-coated balloon for coronary artery disease
This trial is tracking the long-term safety and effectiveness of a sirolimus-eluting balloon (Selution SLR) in people with coronary artery disease. It aims to see how well this device works when used to open blocked arteries in real-world medical practice.
AmadoraAges 18 years+ - NCT06200285Recruiting
Accidental hypothermia registry: tracking causes and treatments
This trial collects information from patients with accidental hypothermia (body temperature at or below 95°F) to learn more about what causes it, who it affects, and how it's treated. There is no experimental treatment—just data gathering. Your story could help researchers improve care for future cases.
InnsbruckAges Any age - NCT06463119Recruiting
Vaccine response registry for immune-weakened patients
This study creates a registry to track how people with weakened immune systems respond to vaccines. It helps doctors better understand which vaccines work best for patients like you.
GenevaAges Any age - NCT04548375Recruiting
Registry study of pain relief from spinal cord stimulation
This is an observational registry that follows people who have a spinal cord stimulation (SCS) implant for approved pain-related conditions. It aims to learn how well SCS works in real-world care, which may help improve treatment and outcomes over time.
Reno, NevadaAges Any age - NCT01909375Recruiting
Joint replacement registry study for people getting new joints
This is a registry study that collects information about people in the US who are getting a total joint replacement. It may help researchers understand outcomes and improve care for patients like you.
Rosemont, IllinoisAges Any age - NCT03125707Recruiting
Registry for adults with certain BCR-ABL1–negative blood cancers
This study keeps a patient registry to collect information about people with specific myeloid blood neoplasms (a type of blood cancer). It helps researchers understand these conditions over time and may improve how patients are cared for in the future.
AugsburgAges 18 years+ - NCT05792033Recruiting
Registry for early T1 bladder cancer after repeat bladder surgery
This study follows people with newly diagnosed early bladder cancer (T1) to better understand outcomes and guide follow-up care. You may be able to join if your cancer is confirmed after a second look bladder procedure and scans show no spread.
ViennaAges 18–90 - NCT01696721Recruiting
Pediatric radiation therapy registry for children under 22
This study is a registry that collects information from children and teens who receive radiation therapy at participating hospitals. It helps researchers learn how radiation is used in pediatrics and may improve future care.
Palo Alto, CaliforniaAges Up to 21 years - NCT07746947Recruiting
Stroke treatment study for medium-sized vessel blockages
This study looks at how well a procedure to remove blood clots from medium-sized brain arteries works for people who have had a severe stroke. It may help improve recovery by treating blockages that are not in the largest arteries.
Indianapolis, IndianaAges 18–85 - NCT07717437Recruiting
Liver cancer registry for patients who had vein embolization
This registry collects medical images and health information from patients with liver cancer or liver metastases who had a procedure to block certain liver veins (PVE/HVE). The goal is to learn more about this technique and help future patients.
Chicago, IllinoisAges 18 years+ - NCT02964364Recruiting
Registry for people with Takayasu arteritis
This is a patient registry that collects information about people with Takayasu arteritis. It helps researchers better understand the condition and how it affects blood flow in the arms and other major vessels.
Beijing, Beijing MunicipalityAges 5–80 - NCT03131531Recruiting
Lymphoid cancer registry for lymphoma and myeloma patients
This study is a cancer registry that collects information from people with lymphoma, Hodgkin disease, or myeloma. It helps researchers understand these cancers better by using real-world patient data.
BergamoAges 18 years+ - NCT03153683Recruiting
Brain and blood clot registry for adults having brain blood tests
This study is a registry, meaning it collects information from people having surgery or procedures for problems involving blood vessels in the brain. It may help researchers better understand brain blood conditions and clots by tracking patterns over time.
Lexington, KentuckyAges 18 years+ - NCT03621137Recruiting
Registry for people with moderate-to-severe eczema
This registry collects information about people with atopic eczema who begin light therapy (phototherapy) or medicine that changes the immune system. It may help doctors better understand how these treatments work in everyday care in the Netherlands.
Amsterdam, North HollandAges Any age - NCT03949972Recruiting
FSGS and MCD patient registry for kidney disease
This study is a registry that collects medical information from people with nephrotic syndrome caused by FSGS or minimal change disease (MCD). It may help doctors better understand these conditions and improve future care, especially by tracking patients over time.
Cologne, North Rhine-WestphaliaAges Any age - NCT03999983Recruiting
Procedure registry for blocked vertebral artery origins
This trial registry collects information on patients treated with a catheter-based procedure for narrowed or blocked vertebral artery openings in the back of the brain. It may help doctors better understand which patients benefit and how treatment is done, but it’s mainly about tracking outcomes and safety.
Jacksonville, FloridaAges 18–90 - NCT04001582Recruiting
UK facial and shoulder muscle disease patient registry
This registry aims to collect health information from people in the UK who have facioscapulohumeral muscular dystrophy (FSHD). It helps researchers better understand the disease and plan future studies.
Newcastle upon TyneAges Any age - NCT04003363Recruiting
Myotonic dystrophy registry to help track your condition
This is a national registry that collects information from people who have (or may soon have) myotonic dystrophy. By joining, you help researchers better understand the disease and may make future studies easier to access.
Newcastle upon TyneAges Any age
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Common questions
- Are there clinical trials for registry?
- Yes. Clin2 currently lists 1,406 recruiting registry studies from the U.S. registry, each rewritten for real people, not researchers, so you can see what it’s testing and who it’s for.
- How do I know if I qualify for a registry trial?
- Each study lists its eligibility criteria — rules about age, diagnosis, and prior treatments. On every Clin2 trial page we explain these in words written for real people and offer a short, optional pre-screen for a fit read. The study team makes the final decision.
- Does it cost anything to join a registry trial?
- Using Clin2 is always free. Many trials cover the cost of the study treatment and related visits; some reimburse travel. The study team explains exactly what’s covered before you decide.
Related conditions
Clin2 helps you find and understand clinical trials and does not provide medical advice. Study data comes from ClinicalTrials.gov. Talk with your doctor about whether a specific trial is right for you.