Clinical trials
Registry clinical trials
Below are recruiting registry clinical trials, each written for real people, not researchers. We’re tracking 1,401 recruiting studies, each written for real people, not researchers, below.
Recruiting studies
- NCT03855592Recruiting
Cancer patients with blood clots: thrombosis and cancer registry
This study is a registry that collects information about blood clot events in people with cancer. The goal is to better understand how often clots happen and what patterns they follow, which can help improve care.
Alcoy, AlicanteAges 18 years+ - NCT03880708Recruiting
Registry for inherited dangerous heart rhythm conditions
This study is a heart rhythm registry for people with inherited conditions that can cause abnormal heart beats. By collecting health and testing information, researchers hope to better understand these conditions and improve care.
Beijing, Beijing MunicipalityAges 1 hour–90 years - NCT03881345Recruiting
Registry for blood clots in legs or lungs
This registry collects information from people who have a blood clot in a leg or a clot in the lung. It helps researchers understand how these conditions are treated in real life.
Moscow, MoscowAges 18 years+ - NCT03887663Recruiting
Chinese Parkinson’s disease patient registry
This study is a registry that collects information from people with Parkinson’s disease to better understand the condition. You may help researchers learn about patterns of symptoms and care over time.
Changzhi, HunanAges Any age - NCT03894228Recruiting
Study of Crohn’s and colitis medicines during pregnancy and breastfeeding
This registry study tracks outcomes for mothers with inflammatory bowel disease (IBD) and their babies during pregnancy and breastfeeding while using IBD medicines. It aims to better understand the safety of these medicines so future pregnancies can be managed more confidently.
Santiago de Compostela, A CoruñaAges 18 years+ - NCT03900221Recruiting
Pregnancy monitoring registry for multiple sclerosis in France
This study follows people who are pregnant and have multiple sclerosis (or related conditions) to better understand what happens during pregnancy. It does not appear to test a new treatment; it mainly collects health and pregnancy information.
AmiensAges Any age - NCT03908463Recruiting
Heart procedure registry for people who get coronary angioplasty
This trial is a registry that collects health information from adults who undergo a heart procedure called coronary angioplasty. It may help researchers understand outcomes and improve care for future patients undergoing similar treatments.
SeoulAges 19 years+ - NCT03910569Recruiting
Takotsubo heart event registry and blood protein study
This study enrolls people who have been diagnosed with Takotsubo (a temporary, stress-related heart condition). It aims to better understand Takotsubo by collecting your medical records and analyzing proteins, which may help improve care in the future.
Los Angeles, CaliforniaAges 18 years+ - NCT03964480Recruiting
Registry for newly diagnosed peripheral T-cell lymphoma patients
This is an observational registry that collects real-world information about people newly diagnosed with peripheral T-cell or certain NK-cell lymphomas. It does not test a new drug, but it helps researchers understand patterns of disease and care, which can guide future studies.
Stanford, CaliforniaAges 18 years+ - NCT03967808Recruiting
Registry for people with kidney failure on dialysis or similar treatment
This study is a kidney disease registry that collects information from people with end-stage kidney failure who are receiving ongoing kidney replacement treatment. It may help doctors better understand kidney disease over time and improve care planning.
NancyAges Any age - NCT03991728Recruiting
TMJ implant registry for adults with a new jaw joint replacement
This registry is for adults getting an artificial (alloplastic) full replacement of the jaw joint (TMJ). It collects real-world information about your implant and care to help improve future outcomes.
São PauloAges 18 years+ - NCT04004286Recruiting
Pain registry and blood sample biobank for eligible service members
This trial is building a pain registry biobank to learn more about pain and how different people experience it. If you’re eligible for care in the Military Healthcare System and can consent, you may be able to contribute your information for future research.
San Diego, CaliforniaAges 18–80 - NCT03374267Recruiting
Urologic cancer registry study
This registry study collects information from people with different types of advanced or high-risk urologic cancers. It helps doctors learn more about how these cancers are treated in real life.
Multiple LocationsAges 18 years+ - NCT07700966Recruiting
Long-term safety registry for EB treatment
This study follows patients who have already received a gene therapy treatment called prademagene zamikeracel for a severe skin condition called recessive dystrophic epidermolysis bullosa (RDEB). The goal is to track long-term safety and health outcomes after treatment.
Palo Alto, CaliforniaAges Any age - NCT04011527Recruiting
Registry for heart stent procedure using rotational atherectomy
This study collects information from people who are having a heart procedure called rotational atherectomy to open blocked heart arteries. It helps doctors better understand how the procedure is used and its outcomes.
Bad SegebergAges 18–100 - NCT04020783Recruiting
Screening registry for high aldosterone causes of high blood pressure
This study enrolls adults with high blood pressure to record who may have “primary aldosteronism,” a hormone-related cause of high blood pressure. It may help clinicians find better ways to screen and diagnose this condition in people like you.
ShanghaiAges 18–65 - NCT04032470Recruiting
Deep brain stimulation registry for essential tremor patients
This study collects information from adults with essential tremor who are getting deep brain stimulation under the hospital’s standard safety guidelines. It may help improve how this treatment is chosen and used for people with tremor over time.
InnsbruckAges 18 years+ - NCT04039061Recruiting
Study registry for people with ADPKD
This trial is a patient registry that collects information from people who have—or might have—autosomal dominant polycystic kidney disease (ADPKD). It may help researchers better understand the condition and improve future studies.
Kansas City, MissouriAges Any age - NCT04040777Recruiting
Cardiometabolic risk registry for adults
This study is a health registry that collects information about risk factors for heart and metabolic problems in adults. It may help doctors better understand who is at higher risk and guide future prevention strategies.
Pilar, Buenos AiresAges 18 years+ - NCT04045587Recruiting
Registry for severe asthma in adults in Canada
This is a research registry that collects health information from adults with severe asthma to better understand how the condition behaves and how treatments are used. You may be able to take part if your asthma is considered severe and is not well controlled.
Edmonton, AlbertaAges 18 years+ - NCT04048993Recruiting
Uses exercise testing to study health in a biobank
This study builds a biobank (a library of health samples and data) using people who can do difficult exercise. It aims to understand how the body works by collecting physical measurements, which may help future research and treatments.
CopenhagenAges 18 years+ - NCT04062500Recruiting
Heart failure patient follow-up study to track health and deaths
This study follows people with heart failure over time to record outcomes like illness course and death, and to understand how treatments affect results. If you have heart failure and can join regular check-ins, your information may help improve future care.
Shanghai, Shanghai MunicipalityAges 18–90 - NCT04064307Recruiting
Register people with myotubular or centronuclear myopathy
This study sets up a patient registry for people diagnosed with myotubular myopathy or centronuclear myopathy. Your information can help researchers better understand these conditions and plan future studies or treatments.
Newcastle upon Tyne, Tyne and WearAges Any age - NCT04071327Recruiting
Pulmonary hypertension registry for patient experiences
This trial is a registry that collects health information from people with pulmonary hypertension to better understand the disease and improve care. You may be asked to share details about your diagnosis and visits, especially soon after you start seeing a specialized PH care center.
Phoenix, ArizonaAges birth+
Hear when a new Registry trial opens
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Common questions
- Are there clinical trials for registry?
- Yes. Clin2 currently lists 1,401 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.