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Effect of Fecal microbiota transplantation in Obese Patients: a Multi-center, Randomized, Controlled Clinical Trial

Effect of Fecal microbiota transplantation in Obese Patients: a Multi-center, Randomized, Controlled Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024760
Enrollment
Unknown
Registered
2019-07-26
Start date
2019-07-15
Completion date
Unknown
Last updated
2019-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Interventions

Sponsors

Department of Endocrinology and Metabolism, Zhujiang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Men and women aged 18-65 years old; 2. The definition of obesity in Chinese adults is based on the "2003 Guidance on Prevention and Control of Obesity in Chinese Adults": 1) BMI 24 to 28 kg/m2 for overweight; 2) BMI>=28kg/m2 for obesity; 3. Moderate weight changes and exercises over the last 30 days (less than 60 minutes of exercise every week); 4. Patient and family voluntarily participate in and cooperate with and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant women or women who are planning to be pregnant during the study, women who are currently in lactating, or who have not received highly effective, medical-approved birth control methods; 2. Combined with malignant tumors, multiple organ dysfunction and other chronic wasting diseases; 3. Severe hypertension,severe cardiovascular and cerebrovascular disease and severe liver/renal dysfunction; 4. Concurrent C. difficile infection or other known infections; 5. Subjects who had a history of FMT; 6. Diarrhea caused by other reasons, including but not limited tube feeding and drug; 7. Those who undergone gastrointestinal surgery (except for appendectomy) or gallbladder surgery; 8. Severe food allergy; 9. Patients with severe neurological, mental or mental disease; 10. Stomach inhalation within 90 days; 11. Patients who take oral probiotics, prebiotics, antibiotics or proton pump inhibitors (PPIs) within 2 weeks or for any reason,during the study period,take antibiotics, or need toal probiotics, opioids, loperamide or diphenoxylate; 12. Patients who have taken or need to take immunosuppressive agents or hormones during use or during the study; 13. Those who take weight-loss drugs within 90 days or who plan to use GLP-1 receptor agonists, or any weight-loss drugs, or participate in a weight loss study or weight loss program during the study; 14. Those who are participating or participating in other clinical trials within 3 months; 15. Patients with severe diabetic complications; 16. Other endocrine diseases expect for type 1 and type 2 diabetes, such as thyroid and special type diabetes; 17. Patients who are judged by the current researcher that they are inappropriate or impossible to cooperate and complete the entire intervention and observer.

Design outcomes

Primary

MeasureTime frame
BMI;

Secondary

MeasureTime frame
Index of glucose metabolism;Serum Lipid;Intestinal flora;body fat;adverse events;

Countries

China

Contacts

Public ContactHong Chen

Department of Endocrinology and Metabolism, Zhujiang Hospital, Southern Medical University

chenhong123@smu.edu.cn+86 020-62782330

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026