Clinical trials
Registry clinical trials
Below are recruiting registry clinical trials, each written for real people, not researchers. We’re tracking 1,399 recruiting studies, each written for real people, not researchers, below.
Recruiting studies
- NCT06030063Recruiting
General Anesthesia for C-section registry study
This study is gathering information from pregnant people who had general anesthesia (being completely asleep) during a C-section. It helps researchers learn more about how to improve care for others in the future.
Little Rock, ArkansasAges 15–55 - NCT06004544Recruiting
Heart screening in pregnant women without symptoms
This study uses echocardiography (an ultrasound of the heart) to check for hidden heart problems in pregnant women who do not have any symptoms. It aims to find issues early and improve care.
Karachi, SindhAges Any age - NCT05845801Recruiting
Study registry for young adults with pancreatic cancer
This study is a registry, meaning it collects information about young adults diagnosed with pancreatic cancer. It may help researchers better understand this cancer in younger people and improve future care.
VeronaAges 18–55 - NCT05915299Recruiting
Heart surgery donor heart monitoring registry
This is a registry that collects information about how donated hearts are handled using a portable machine that keeps the heart healthy outside the body. It may help researchers improve future care, but it usually does not test a new medication.
Phoenix, ArizonaAges Any age - NCT05694663Recruiting
Vagus nerve stimulation to aid stroke recovery
This registry looks at people with a prior ischemic stroke to see how a device that stimulates the vagus nerve may support arm recovery. If you are planning to get the implant and can follow the program steps, your information may be followed to track progress and safety.
New York, New YorkAges 18 years+ - NCT05843500Recruiting
CTEPD and CTEPH registry for long-term blood-clot lung disease
This study builds a registry to learn about people with chronic blood-clot lung disease (CTEPD/CTEPH) and what symptoms and test results look like over time. It may help clinicians better understand the condition and improve future care, since your participation supports data collection rather than a new drug.
San Francisco, CaliforniaAges 18 years+ - NCT05489393Recruiting
Global registry for people with DRPLA
This study is a global patient registry that collects information from people with DRPLA to better understand the condition over time. It may help researchers learn what to expect and how to support future treatments, and participation mainly involves giving consent and sharing your history.
New York, New YorkAges birth–100 years - NCT05329935Recruiting
Registry for children with congenital thymus missing
This registry follows children born with congenital athymia (a missing or non-working thymus). It collects information around treatment with RETHYMIC, which may help researchers better understand how care and outcomes look over time.
Durham, North CarolinaAges birth–21 years - NCT05332249Recruiting
Registry for Degenerative Spine Disease in the Neck and Low Back
This study is a registry (a way to collect health information) for people with wear-and-tear (“degenerative”) problems in the neck and/or low back. It may help doctors better understand these conditions and improve future care plans.
Seoul, KoreaAges 18–100 - NCT05630989Recruiting
Registry for outcomes in KRAS G12R pancreatic cancer on MEK therapy
This study keeps a registry (a secure database) to track how people with advanced pancreatic cancer and a KRAS G12R mutation do after treatment with a MEK inhibitor–based combination. It helps doctors understand which outcomes matter most for this specific genetic type of cancer.
Milwaukee, WisconsinAges 18 years+ - NCT04853732Recruiting
Pain research registry for chronic low back pain
This study is a research registry that collects information from people with chronic low back pain (and some people without chronic pain). It may help researchers better understand pain patterns and guide future treatments.
Fort Worth, TexasAges 21–79 - NCT05179863Recruiting
Swiss rare disease registry for patients and caregivers
This study builds a “registry,” which is a secure list of people with rare diseases or suspected rare diseases in Switzerland. It helps researchers better understand these conditions over time and improve care.
AarauAges Any age - NCT05102916Recruiting
Registry for neuromuscular disorder patients in Switzerland
This study is a patient registry that collects health information from people diagnosed with a neuromuscular disorder in Switzerland. It helps researchers better understand these conditions and how they vary from person to person.
Aarau, Canton of AargauAges birth+ - NCT04954404Recruiting
Mitral valve procedure registry for Chinese patients in one center
This study is a registry (a way to track real-world outcomes) for people with mitral valve disease who receive a mitral valve procedure. It helps doctors understand how well these procedures work and what complications happen in patients like you.
Hangzhou, ZhejiangAges 18 years+ - NCT05077124Recruiting
CytoSorb safety registry for clot-fighting medicine removal
This registry collects information on people who use CytoSorb to remove clot-fighting medicines from the blood. It’s mainly meant to track safety and how quickly the removal works, which may help improve care for future patients.
GrazAges 18 years+ - NCT04670172Recruiting
Chronic sinusitis patient registry using a phone app
This study builds a real-world record of symptoms and outcomes in people with chronic sinusitis. You may help by using a smartphone app to report your symptoms over time.
GrazAges 18 years+ - NCT04725422Recruiting
Registry for children with nonbacterial bone inflammation
This study collects medical information (and imaging results) from children and teens with nonbacterial bone inflammation. It may help doctors better understand how this condition looks on scans and how it’s diagnosed, especially to rule out infection or cancer.
Seattle, WashingtonAges Up to 21 years - NCT05072119Recruiting
Hospital registry to track heart device outcomes
This study keeps a secure record of people who receive a pacemaker, ICD, or implantable loop recorder, to understand how these devices perform over time. If you join, your care team will track your follow-up visits for at least 12 months.
Naples, NapoliAges 14 years+ - NCT04098146Recruiting
Registry for jawbone reconstruction after jaw cancer and jaw bone death
This study collects real-world information from people undergoing jaw reconstruction after their jaw bone was damaged (from cancer and certain medicines). It may help improve future treatment planning by tracking surgical choices and outcomes.
Jacksonville, FloridaAges 18 years+ - NCT04282083Recruiting
Registry for adults with confirmed digestive neuroendocrine tumors
This is a registry study that collects medical information from adults with neuroendocrine tumors (NETs) that start in the digestive organs. It helps researchers understand these cancers better and may support future studies.
Rozzano, MilanAges 18 years+ - NCT04438889Recruiting
Join the Austrian myeloid patient registry
This is a registry study that collects information from people with myeloid blood diseases. It helps researchers better understand these conditions and support future research.
FeldkirchAges 18 years+ - NCT04487314Recruiting
Study of chronic vein disease over time
This study follows people (and certain close family members) to document how chronic vein problems develop and change over time. You would get yearly checkups and ultrasound scans to track the natural course of the condition.
Saint PetersburgAges 10 years+ - NCT04220970Recruiting
Breast implant lymphoma patient registry
This study is a registry that collects information from adults diagnosed with lymphoma that may be linked to breast implants. It helps researchers understand the condition better and may guide future care.
BrugesAges 18 years+ - NCT03057860Recruiting
Registry study for moderate to severe atopic dermatitis in Germany
This study is a national registry that collects information from people with moderate-to-severe atopic dermatitis (eczema). It helps doctors understand what treatments are used and how patients are doing over time.
Hanover, Lower SaxonyAges Any age
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Common questions
- Are there clinical trials for registry?
- Yes. Clin2 currently lists 1,399 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.