Clinical trials
Registry clinical trials
Below are recruiting registry clinical trials, each written for real people, not researchers. We’re tracking 1,390 recruiting studies, each written for real people, not researchers, below.
Recruiting studies
- NCT02245763Recruiting
Mitral valve procedure registry for patients who can take blood thinners
This is a study that collects medical information about people having a mitral valve procedure, to better understand outcomes. It may help because it improves how doctors choose and manage care for mitral valve problems.
Washington D.C., District of ColumbiaAges 1 year+ - NCT02325674Recruiting
Metreleptin safety and effectiveness registry
This registry follows people who are already taking metreleptin (a medicine for certain rare conditions) to better understand its long-term safety and how well it works in everyday use. It may help you and other patients by building real-world evidence about this treatment.
Birmingham, AlabamaAges Any age - NCT02270567Enrolling by invitation
Registry study for neuroendocrine tumors in patients worldwide
This study keeps a worldwide record of people with neuroendocrine tumors to learn about care patterns and outcomes. It may help your doctors and future patients by improving how these tumors are monitored and treated.
Branford, ConnecticutAges 18 years+ - NCT02306720Enrolling by invitation
Patient registry for hypophosphatasia (HPP)
This trial is a registry that collects information about people with hypophosphatasia to help researchers understand the condition better. It may help future studies, but it’s not a treatment trial.
Centennial, ColoradoAges Any age - NCT01402661Enrolling by invitation
Rheumatoid arthritis drug safety and effectiveness registry
This registry collects real-world information about people with rheumatoid arthritis (RA) to help doctors understand how RA medicines work and their safety. You may be able to join if you’re newly diagnosed or starting certain RA treatments and you’re willing to share consent and basic personal details.
Waltham, MassachusettsAges 18 years+ - NCT01772602Recruiting
Join a national ALS patient registry in the U.S.
This study is a national registry that collects information from people with amyotrophic lateral sclerosis (ALS) to better understand the disease. Joining may help researchers learn about patterns of symptoms and care over time.
Atlanta, GeorgiaAges 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+ - NCT01633489Recruiting
LAL deficiency patient registry
This study keeps a protected record of people with Lysosomal Acid Lipase (LAL) deficiency to learn more about the condition over time. It may help researchers better understand how patients are doing and support future studies.
Phoenix, ArizonaAges Any age - NCT01524276Recruiting
Registry to track outcomes of Medtronic medical devices
This is a follow-up registry that collects information from people who have (or will receive) an eligible Medtronic device. It helps the company and doctors better understand how the device works in real-world use.
Birmingham, AlabamaAges Any age - NCT02087852Recruiting
Kidney cancer DNA registry for patients and family
This study collects DNA from adults with kidney cancer (or suspected kidney cancer), plus DNA from some family members and healthy controls. It helps researchers understand whether certain genetic changes might be linked to kidney cancer risk.
Basking Ridge, New JerseyAges 18 years+ - NCT01409109Recruiting
Study database for brain signal markers in psychosis
This study builds a database of brain-signal measurements to help find “biomarkers” that may point to schizophrenia or related mental illnesses. Depending on whether you have a mental health diagnosis or you’re healthy, the study will collect information and brain data to compare groups.
Dallas, TexasAges 18–60 - NCT01904851Recruiting
Registry for leg artery procedures and their outcomes
This study collects information about people who had a procedure to improve blood flow in certain leg arteries. It helps researchers understand which treatments work best and what outcomes to expect.
Little Rock, ArkansasAges Any age - NCT01577251Recruiting
Cancer patients on radiation can join a registry
This study builds a registry and blood/tissue sample collection for people who have cancer or a non-cancer growth (benign tumor) and are receiving radiation. It helps researchers learn from real-world treatment and biology, which may improve future care.
Moorestown, New JerseyAges 18 years+ - NCT01915511Recruiting
Long-term registry for new or worsening lung scarring
This study collects health information over time from people with newly diagnosed idiopathic pulmonary fibrosis (IPF) or other lung scarring diseases that are getting worse. It’s meant to better understand disease patterns and outcomes, which may help doctors plan future care.
Birmingham, AlabamaAges 21 years+ - NCT01694940Recruiting
Mitochondrial disease registry and sample collection study
This trial builds a large database and collection of lab results, and possibly tissue samples, from people with suspected or diagnosed mitochondrial conditions. It helps researchers learn more about these disorders and mitochondrial DNA changes, which may improve future diagnosis and treatments.
San Diego, CaliforniaAges Any age - NCT01759225Enrolling by invitation
Registry study of people with heart and blood vessel disease
This is a registry (a study that collects health information) for people with certain heart and blood vessel conditions. It may help researchers better understand who has these diseases, how they are managed, and outcomes over time.
Tel AvivAges Any age - NCT01761981Recruiting
Registry for patients with hereditary bleeding vessel disease (HHT)
This is a patient registry that collects information about people with hereditary hemorrhagic telangiectasia (HHT). It may help doctors better understand the condition and improve care over time.
Buenos Aires, Buenos AiresAges 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 - NCT01779115Enrolling by invitation
Diabetes registry for people with diagnosed high blood sugar
This is a research registry that collects information from people who have diabetes (high blood sugar on tests or based on diabetes treatment). It may help researchers understand diabetes patterns in a real-world healthcare system.
Tel AvivAges Any age - NCT02038127Recruiting
Heart procedure outcomes tracking registry
This study collects information from people having a heart procedure called percutaneous coronary intervention, or PCI, to learn more about their outcomes and improve future care.
Chuncheon, Gangwon-doAges Any age - NCT02165059Recruiting
Stomach and small-bowel tissue study during surgery
This study collects small tissue samples from the stomach and upper small intestine while you’re already having certain kinds of GI (digestive) or abdominal surgery. It aims to learn what causes stomach or bowel movement problems in some patients, which could guide future diagnosis and care.
Indianapolis, IndianaAges 6 months–90 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+ - 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+ - NCT01822470Enrolling by invitation
Registry studying bacteria patterns in suspected small bowel overgrowth
This is a research registry that collects small-bowel fluid samples from people being tested for “SIBO” (an overgrowth of bacteria in the small intestine). It aims to describe what bacteria are present and how results differ between people with suspected SIBO and others having similar tests for other reasons.
Indianapolis, IndianaAges 18–90
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Common questions
- Are there clinical trials for registry?
- Yes. Clin2 currently lists 1,390 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.