Chemotherapy-induced Diarrhea

2

Review clinical trials related to Chemotherapy-induced Diarrhea. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Inactivated Bacteroides Fragilis for Prevention of Chemotherapy-Induced Diarrhea

The incidence of chemotherapy-induced diarrhea (CID) is closely related to the types of anticancer drugs. Combination chemotherapy regimens such as fluorouracil derivatives and irinotecan, as well as tyrosine kinase inhibitors like neratinib, are associated with a high severity and incidence of diarrhea. These All antineoplastic agents can induce intestinal epithelial cell apoptosis, damage the intestinal mucosa, subsequently reduce the absorption surface area, and thereby lead to diarrhea. Recent literature has indicated that Bacteroides fragilis may be a candidate drug for the treatment and prevention of CID. This study intends to conduct a randomized controlled trial to determine the efficacy and mechanism of action of inactivated Bacteroides fragilis (SK10) in the prevention of chemotherapy-induced diarrhea (CID).

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen Hospital of Southern Medical UniversityUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Voluntarily sign the informed consent form, be able to comply with the protocol... [+7]

History of altered bowel habits or abnormal stool characteristics prior to scree... [+13]

Status: Recruiting

Probiotics for Abemaciclib-Induced Abdominal Discomfort.

This study aims to evaluate whether the addition of probiotics can help reduce abdominal discomfort (such as diarrhea) in breast cancer patients receiving Abemaciclib treatment. Abemaciclib is an effective targeted therapy but often causes gastrointestinal side effects. While Loperamide is the standard treatment for diarrhea, this study explores if probiotics can provide additional relief and improve metabolic health.Participants will be randomly assigned to receive either probiotics or a placebo alongside their standard care. The study will monitor the frequency of abdominal symptoms and analyze blood samples to observe changes in metabolic factors.

Participants needed: 80
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Leeuwenhoek Laboratories Co. Ltd.Updated: May 26, 2026Locations: 1
Eligibility criteria

Absolute Neutrophil Count (ANC) ≥ 1,500/μL without G-CSF support within 14 days... [+4]

Severe renal impairment (e.g., estimated creatinine clearance < 30 mL/min). [+4]