Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
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]

Status: Not yet recruiting

Effects of Synbiotics on Obesity

Synbiotics are a combination of probiotics and prebiotics that can promote the survival of probiotics in the gut. Probiotics utilize prebiotics to produce various metabolites beneficial to human health, such as short-chain fatty acids. The purpose of this trial is to evaluate the impact of a synbiotics product developed by Leewenhoek Laboratories Co., Ltd., on human obesity and its related biomarkers. Participants will be randomly assigned to either the experimental group or the control group in a double-blind trial. The intervention involves the experimental group taking the synbiotics product twice daily, two capsules per dose, after meals for six weeks. The control group will take an equal amount of placebo daily. During the trial, participants' body weight will be recorded weekly, and their body weight, waist circumference, hip circumference, body fat composition, and skeletal muscle mass will be measured before and after the intervention. Additionally, fasting blood samples and blood samples collected at 30, 60, 90, and 120 minutes after consuming the nutritional supplements will be analyzed. The study will compare body fat percentage, body weight, BMI, waist circumference, hip circumference, skeletal muscle mass, and obesity-related biomarkers in blood between the experimental and control groups. The trial results will be used to assess the efficacy of the synbiotics product in improving obesity and its related biomarkers.

Participants needed: 80
Trial details
Phase: Phase 2Age: 20-60Biological sex: AllType: InterventionalSponsor: Leeuwenhoek Laboratories Co. Ltd.Updated: Oct 9, 2024
Eligibility criteria

Age between 20-60 years. [+10]

Pregnant or breastfeeding. [+6]

Status: Not yet recruiting

Investigation of Metabolomics Differences Between Metabolic Syndrome and Healthy Individuals in Taiwan

The prevalence of metabolic syndrome in Taiwan has been increasing yearly. In this project, the database of blood test results from healthy and metabolic syndromes individuals will be analyzed to identify the small molecules related to the severity of metabolic syndrome. These identified small molecules could be used as biomarkers to predict the development of metabolic syndromes in the future.

Participants needed: 1,200
Trial details
Age: 20+Biological sex: AllType: ObservationalSponsor: Leeuwenhoek Laboratories Co. Ltd.Updated: Apr 12, 2024
Eligibility criteria

Capable adults weigh ≥ 50 kg

Not Taiwanese [+4]