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Clinical Trials in Egypt / NCT06783153
Starting soon Phase 1/2

Efficacy and Safety of Adjunctive Use of Rifaximin In Preventing Radiotherapy-induced Diarrhea in Cancer Patients

NCT06783153 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 1/2
Started
2025-01-20
Last updated
2025-01-20

Condition(s) studied

Radiotherapy Induced DiarrheaAcute Radiation EnteritisProstate CancerCervical AdenocarcinomaBladder (Urothelial, Transitional Cell) CancerRectal AdenocarcinomaPelvic RadiotherapyRifaximin

Investigational drug(s) / intervention(s)

Rifaximin 550 MG →Standard Care Chemoradiation

Rifaximin 550 MG: Oral Rifaximin 550mg twice daily from the start of pelvic radiotherapy, with or without chemotherapy, as a preventive measure, and continuing every day until the end of the treatment up to 5 to seven weeks.

Standard Care Chemoradiation: Patients will receive standard chemotherapy and/or radiation

Study summary

Preclinical data indicate that rifaximin could be repurposed as a novel strategy for preventing and reducing the severity of gastrointestinal damage, particularly diarrhea, that results from pelvic irradiation. So, The aim of the work is to investigate the impact of Rifaximin on the incidence and severity of radiotherapy-induced diarrhea in cancer patients undergoing pelvic irradiation with or without chemotherapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Individuals who are 18 years of age or older and have been diagnosed with non metastatic pelvic cancers. * Patients who are undergoing curative intent radiotherapy with or without chemotherapy treatment. Exclusion Criteria: * Patients who have a record of intestinal resection in their medical history. * Patients with a medical background of irritable bowel syndrome. * Patients with a history of inflammatory bowel disease. * Patients who regularly take anti-diarrheal medications before commencing radiotherapy. * Patients experiencing diarrhea at the outset of the study. * Patients with compromised immune systems, such as those who are HIV positive or using immunosuppressive medications. * Pregnant or lactating woman. * Patients allergic to rifamycin.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mansoura University Al Mansurah Province

More Mansoura University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06783153 on ClinicalTrials.gov ↗ ← All trials in Egypt