Clin2
NCT04700527Possibly a fitRecruiting

Nutritional supplement for reducing side effects from radiation to the belly or pelvis

ToxicityRadiation Toxicity

Part of Cancer, Digestive system, Injuries & trauma clinical trials.

This trial is studying whether a nutritional supplement (a type of short-chain fatty acid) can help reduce the side effects of radiation therapy for cancers in the abdomen or pelvis. It aims to improve quality of life during treatment.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
122 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Diagnosed with a gastrointestinal, urologic, or gynecologic cancer (including sarcoma).
  • Scheduled to receive a minimum dose of radiation to the abdomen or pelvis.
  • 18 years or older with an ECOG performance status of 0-2 (able to carry out daily activities and light chores).
  • No history of inflammatory bowel disease (like Crohn's or ulcerative colitis), chronic diarrhea, or a severe nut allergy.
  • Women of childbearing potential must have a negative pregnancy test and use effective contraception; men with partners of childbearing potential must use contraception.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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