Clinical trial Recruiting at 1 site Observational

GIST Patient Registry for real-world insights

Official title: Life Raft Group GIST Registry Protocol

Run by The Life Raft Group · NCT07697248 · Data updated 2026-11-12

This registry collects medical information from people with GIST to see how the disease behaves in real life and to help improve care.

More GIST trials

Quick facts

Study typeObservational
SexAll
Enrollment5000 (estimated)
SponsorThe Life Raft Group
Academic / other
Locations1 site (Wayne, New Jersey)
StatusRecruiting
StartedApril 2013
Main results expectedDecember 31, 2099
Study endsDecember 31, 2099
Registry record updatedJuly 13, 2026
Trial IDNCT07697248 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals diagnosed with GIST who can provide informed consent and willing to share medical information for research.

Probably not a fit

Patients who do not wish to share their medical information or who do not meet consent requirements may not benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The Life Raft Group GIST registry is an observational database that gathers medical information from individuals diagnosed with GIST and related cancers. It aims to improve understanding of disease patterns, outcomes, and potential links to treatments or molecular targets. Data may come from medical records, surveys, and a linked tissue bank, with separate consent required for tissue samples. Participation involves providing consent and sharing information; joining the registry does not require involvement in other LRG activities. The registry facilitates research by aggregating real-world experiences to support future studies and patient care improvements.

Why it matters

Potential benefit: Participants may contribute to research that could enhance understanding and management of GIST and related illnesses, potentially benefiting future patients.

How similar studies have gone: Other disease registries have successfully used real-world data to inform understanding and care, though this specific registry is observational and focused on GIST.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Gastrointestinal Stromal Tumor diagnosis
2. Provide written and informed consent

Exclusion Criteria:

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Where it's running

  • The Life Raft Group
    Wayne, New Jersey, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.