Clinical trials
Registry clinical trials
Below are recruiting registry clinical trials, each written for real people, not researchers. We’re tracking 1,405 recruiting studies, each written for real people, not researchers, below.
Recruiting studies
- NCT00512694Recruiting
Duke lupus registry for people with lupus
This trial is a registry that follows people with lupus to help Duke researchers learn about the disease and care. You may be able to join if you’re seen by a Duke rheumatologist and can come to follow-up visits.
Durham, North CarolinaAges 18 years+ - NCT01246765Recruiting
Pregnancy medication registry for mental health medicines
This study helps track how psychiatric (mental health) medicines affect pregnancy outcomes by collecting phone interviews during pregnancy. If you are pregnant and take (or have taken) mental health medication, you may help doctors understand risks and benefits better.
Boston, MassachusettsAges 18–45 - NCT01158482Recruiting
Track outcomes after placing or removing an IVC filter
This study follows adults who are getting an IVC filter placed or removed. It aims to better understand how patients do after the procedure, both in the short term and longer term.
Stanford, CaliforniaAges Any age - NCT01756222Recruiting
Bicuspid aortic valve registry for adults
This study is a registry that collects health information from adults with bicuspid aortic valve disease. It may help doctors better understand outcomes and guide future care for patients and families affected by this condition.
Ann Arbor, MichiganAges 18 years+ - NCT01534299Recruiting
Registry study for kidney nerve treatment candidates
This is a study that collects information from people who may receive a kidney-nerve procedure to help treat high blood pressure. If you qualify as a candidate and consent, the study helps doctors understand how the treatment is used in real-world care.
Homburg, SaarlandesAges 18 years+ - NCT02038127Recruiting
Health registry for people getting a drug-coated heart stent
This study follows people who need a coronary (heart) stent to see how they do after treatment. It does not sound like an experimental drug trial for you—it’s mainly about collecting health information after a stent procedure.
Chuncheon, Gangwon-doAges 19 years+ - NCT00258583Recruiting
ILD patient registry at UPMC Simmons Center
This study is a registry that collects information from adults with interstitial lung disease (ILD) who are seeking care at the UPMC Simmons Center. It helps the center learn about ILD and improve future treatment planning.
Pittsburgh, PennsylvaniaAges 18 years+ - NCT01408225Recruiting
Myeloma and amyloidosis patient data and sample registry
This study collects health information and, if needed, samples from people diagnosed with certain blood disorders related to plasma cells. Sharing your information may help researchers better understand these diseases and improve future care.
Columbus, OhioAges 18 years+ - NCT01514045Recruiting
Gastric cancer registry for patients and certain family members
This study builds a registry (a secure database) to learn about people with gastric cancer, people at higher risk because of family history, and people with a specific inherited gene change. Being in the registry may help researchers understand causes and improve future care.
Stanford, CaliforniaAges 18 years+ - NCT00231400Recruiting
Pompe disease registry for people with confirmed diagnosis
This trial is a registry, meaning it collects health information from people with confirmed Pompe disease. It may help researchers better understand the disease and improve future treatments.
Birmingham, AlabamaAges Any age - NCT01808937Recruiting
Study registry for morphea and storing DNA samples
This study is building a registry (a group record) of people with morphea and collecting DNA samples to help researchers learn more about the condition. It may help by improving understanding of causes, patterns, and future treatments.
Dallas, TexasAges Up to 90 years - NCT01733082Recruiting
Mycophenolate pregnancy registry for mothers in the U.S.
This study collects information about pregnancies where a mother took mycophenolate during pregnancy (or stopped within the prior 6 weeks). It aims to better understand pregnancy outcomes and risks so care can be improved for future patients.
Cambridge, MassachusettsAges Any age - NCT01179815Recruiting
Join the Swiss diabetes registry study for adults
This study keeps a registry (a secure list) of adults with diabetes. It collects information over time to better understand diabetes and support care—your participation is voluntary.
BernAges 18 years+ - NCT00178724Recruiting
Spinal cord injury registry for people after a first trauma
This trial is a registry that collects information about people 18 and older who have a first spinal cord injury caused by trauma. By sharing details, you help researchers better understand outcomes and care needs after these injuries.
Miami, FloridaAges 18 years+ - NCT02038660Recruiting
Drug-coated balloon treatment registry for narrowed blood vessels
This study records outcomes for people who get a drug-coated balloon used to treat a narrowed blood vessel after a first balloon treatment. It may help doctors understand how well this approach works in everyday care and for different patient needs.
Bucheon-siAges 20 years+ - NCT00477100Recruiting
Breast cancer tissue and data registry for research
This trial helps create a research “tissue registry” by collecting breast cancer tissue samples and medical information. It may help doctors better understand inflammatory or invasive breast cancer and improve future studies.
Gilbert, ArizonaAges 18 years+ - NCT00455104Recruiting
Fabry disease registry for Canadians and eligible adults
This study is a national registry that collects health and medical information from people with Fabry disease. It helps researchers better understand the condition and plan future care and studies.
Calgary, AlbertaAges 5–85 - NCT01848028Recruiting
German registry collecting data on new systemic psoriasis treatments
This study is a psoriasis registry that records real-world information about people starting a systemic (whole-body) treatment for the first time. It helps doctors understand how these treatments work in everyday care and may improve future treatment decisions.
HamburgAges 18 years+ - NCT01390675Recruiting
Registry for heart valve replacement anesthesia during TAVR
This study tracks patients who get a transcatheter aortic valve implantation (TAVR), a procedure to replace a narrowed heart valve without open-heart surgery. It looks at the type of anesthesia used during the procedure and records outcomes to learn what works best for patients.
Munich, BavariaAges 18 years+ - NCT01965132Recruiting
Biologic and targeted therapy registry for arthritis patients
This registry is collecting information about people with rheumatoid arthritis, ankylosing spondylitis, or psoriatic arthritis who are starting or needing biologic or targeted medicines. It may help researchers better understand how these treatments work in real life.
SeoulAges 18 years+ - NCT01062581Recruiting
Study of organ transplants done at University of Minnesota
This registry study collects information about people who received an organ transplant at the University of Minnesota and about living donors who donated there. It helps researchers learn from transplant experiences to improve care.
Minneapolis, MinnesotaAges Any age - NCT00260585Recruiting
Esophageal risk and tissue registry study
This study collects information and, if you already need blood tests or procedures, may take extra small tissue samples (biopsies) to better understand esophageal-related conditions. It may help researchers learn about risk and future management for people with certain esophagus or reflux-related diagnoses.
Pittsburgh, PennsylvaniaAges 18 years+ - NCT01522183Recruiting
Registry for people with atypical hemolytic uremic syndrome
This is a registry that collects information from people diagnosed with atypical hemolytic uremic syndrome (aHUS). It helps researchers better understand the condition across different genetic causes and treatment needs.
Aurora, ColoradoAges Any age - NCT00307281Recruiting
Emphysema and COPD patient registry with sample storage
This study enrolls people who have emphysema/COPD into a research registry and collects health information and biological samples. It may help researchers understand the disease better and improve future treatments.
Pittsburgh, PennsylvaniaAges 21 years+
Hear when a new Registry trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.
Common questions
- Are there clinical trials for registry?
- Yes. Clin2 currently lists 1,405 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.