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
- NCT07166172Recruiting
Long-term outcomes after fetal surgery for severe CDH
This study follows pregnant women and their babies after a special fetal surgery (FETO) for severe diaphragmatic hernia (CDH). It aims to understand long-term health outcomes for both mother and child.
Baltimore, MarylandAges 18 years+ - NCT07172243Recruiting
Amycon biobank and data registry for amyloidosis
This study collects blood and tissue samples and health data from people with amyloidosis to build a biobank and registry. Researchers hope this will help improve future diagnosis and treatment.
LeuvenAges 18 years+ - NCT07174362Recruiting
Heart failure study for newly diagnosed patients
This study is tracking people who were recently diagnosed with heart failure and have a weakened heart pumping function (less than 50%). It aims to learn more about the condition and improve care.
Basildon, EssexAges 18 years+ - NCT07171242Recruiting
Stroke patient registry study
This study is a registry that collects information from people who have had an ischemic stroke (a type of stroke caused by a blocked blood vessel in the brain). By tracking this information, researchers hope to better understand the condition and improve care for future patients.
Shanghai, Shanghai MunicipalityAges 18 years+ - NCT07163416Recruiting
Italian migraine registry study for adults
This study tracks people with migraine to learn more about their condition and improve care. You may join if you have episodic or chronic migraine, with or without aura or medication overuse headaches.
Roma, RomaAges 18 years+ - NCT07160023Recruiting
Registry study for primary cutaneous T-cell lymphoma
This study follows people with primary cutaneous T-cell lymphoma who are seen at the Dermatology Unit in Pavia. It collects information to better understand the disease and improve care.
Pavia, PaviaAges 6 years+ - NCT07159165Enrolling by invitation
Registry study of MIUS for enlarged prostate
This study collects information from men treated with a minimally invasive surgery called MIUS for an enlarged prostate that blocks urine flow. It aims to learn how well the procedure works by tracking results over time.
SamsunAges Any age - NCT07156851Recruiting
Belgian registry of implanted EV-ICD devices
This study registers patients who have had or will have an extravascular implantable cardioverter-defibrillator (EV-ICD) placed. It aims to track how the device performs and any complications in real-world use.
AntwerpAges 18 years+ - NCT07161583Recruiting
Advanta VXT and Flixene Graft Registry
This registry follows people who have already received an Advanta VXT or Flixene graft to repair or replace a peripheral artery. It collects information from medical records to see how the grafts perform over time.
Boston, MassachusettsAges 18 years+ - NCT05213429Recruiting
Coronary artery ectasia registry for people getting heart angiograms
This study is a registry (a structured way of collecting health information) for people suspected of coronary artery disease who are having an elective heart angiogram. It helps researchers better understand coronary artery ectasia and how it shows up in everyday patients.
AmmanAges 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+ - NCT06957613Recruiting
A Registry for Chronic Total Heart Artery Blockages
This study is collecting information on people who have a complete blockage in a heart artery (a chronic total occlusion) and who are scheduled for a procedure to open it up. The goal is to learn more about the treatment and outcomes for these patients.
Bad Segeberg, Schleswig-HolsteinAges 18–100 - NCT07154758Recruiting
Optimizing heart failure treatment using registry data
This trial uses a national heart failure registry to see if a new way of monitoring treatment can help optimize therapy for people with heart failure and reduced ejection fraction (a weak heart pump). It may lead to better medication adjustments over time.
GothenburgAges Any age - NCT07146256Recruiting
OPMD Natural History Registry Study
This study is building a national registry (a database) for people with Oculo-Pharyngeal Muscular Dystrophy (OPMD) in Israel. Joining will help researchers understand how OPMD progresses over time and may lead to better care.
Ramat GanAges 18 years+ - NCT07154654Recruiting
Long-term study of mexiletine in young children with myotonic disorders
This study follows children under 6 years old with genetic myotonic disorders who are taking or may take mexiletine. It helps doctors understand how well the medicine works and if it is safe over time.
Clermont-FerrandAges Up to 6 years - NCT07154823Recruiting
Blood cancer registry study for biomarker discovery
This study collects samples and health information from people with certain blood cancers to learn more about the disease and find markers that may help guide future treatments. You will not receive a treatment from this study, but you may help advance research.
Iowa City, IowaAges birth+ - NCT07155148Recruiting
Argentine registry for Crohn's and colitis patients
This study collects information from people diagnosed with inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis. By joining the registry, you help researchers learn more about these conditions and improve care.
Córdoba, Córdoba ProvinceAges Any age - NCT07145138Recruiting
Multi-ethnic dilated cardiomyopathy registry
This study is a registry for people with dilated cardiomyopathy (DCM)—a condition where the heart's main pumping chamber becomes enlarged and weak. It aims to learn more about DCM, especially in people from different ethnic backgrounds, by collecting health information over time.
Chicago, IllinoisAges 18 years+ - NCT07149701Recruiting
Ventricular Tachycardia patient registry study
This study is for adults with ventricular tachycardia (a fast heart rhythm) who also have structural heart disease. It will track your health over time to learn more about how this condition is managed.
BeijingAges 18 years+ - NCT07149688Recruiting
Heart disease health program for older adults in Qujiang
This study follows older adults in Qujiang District who have chronic heart or blood vessel conditions. It aims to improve care through village-based management and help researchers better understand how to support long-term heart health.
Beijing, Beijing MunicipalityAges 60 years+ - NCT04776824Recruiting
Swiss registry for people with amyloidosis and possible heart involvement
This trial is a registry that collects health information from people with amyloidosis, including cases where the heart may be involved. Sharing your medical details can help researchers learn how this condition affects patients and may guide future care.
BaselAges 18 years+ - NCT06726109Recruiting
FOCUS study on acute heart failure
This trial is studying patients admitted to the hospital for acute heart failure. It will collect information to better understand and treat people with low heart pumping strength (ejection fraction less than 40%) and fluid retention.
Genk, BelgiumAges Any age - NCT06952400Recruiting
Melanoma genetics study in Taiwan
This study looks at genetic changes in melanoma tumors to better understand the disease. It may help find the best treatments for different stages of melanoma.
Taipei, Taiwan/TaipeiAges 18 years+ - NCT06958341Recruiting
Brain and nerve disease registry with optional fluid collection
This study collects extra fluid from a spinal tap to learn more about brain and nerve diseases. It may help find better treatments in the future.
Berlin, State of BerlinAges Any age
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 1,390 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.