Clin2
NCT07164534Worth exploringNot yet recruiting

Supplement to reduce radiation side effects in cervical cancer

Uterine Cervical Neoplasm

Part of Cancer, Women’s health & pregnancy clinical trials.

This trial tests whether an oral supplement called sodium-copper chlorophyllin can reduce long-term side effects from radiation therapy in women with cervical cancer. It is designed for people whose radiation plan delivers a higher dose to the rectum or bladder than usually recommended.

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

Phase
Phase 3
Enrollment
316 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have cervical cancer (the squamous or glandular type) that has not spread far and are scheduled for radiation therapy, usually with chemotherapy.
  • Your radiation plan gives a higher than usual dose to the rectum or bladder, and you are willing to take an extra oral supplement to help protect these areas.
  • You are 18 or older and can swallow tablets.
  • Your blood counts, kidney, liver, and blood clotting tests are within acceptable ranges.
  • You are not HIV positive, not taking blood thinners, and have not had another cancer or radiation treatment that could interfere.

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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