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Efficacy evaluation of compound eosinophil-lactobacillus tablets in patients after colonoscopy

Efficacy of compound eosinophil-lactobacillus tablets on reducing the incidence of diarrhea in patients after colonoscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031382
Enrollment
Unknown
Registered
2020-03-29
Start date
2020-03-28
Completion date
Unknown
Last updated
2020-04-13

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

Conditions

Intestinal dyabacteriosis

Interventions

control group:Routine gastrointestinal tract preparation
experimental group:Routine gastrointestinal tract preparation and oral compound eosinophil-lactobacillus tablets 14 days after colonoscopy

Sponsors

Suzhou Ninth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who voluntarily sign informed consent; 2. Men and women over 18 years old; 3. Outpatients who need to have a colonoscopy.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic or local malignant tumors or patients who cannot stop immunosuppressive drugs; 2. patients with chronic diarrhea, inflammatory bowel disease, infectious gastrointestinal disease, functional constipation, and partial intestinal polyps (a. Size >= 2cm,b number of polyps > 3, and c need EMR treatment, if any one or more of them are met, they will be excluded); 3. Abnormal stool routine results: fecal occult blood (+) or leukocyte (+); When fecal occult blood (+), but colonoscopy results are normal, can be included in this study; 4. Patients with severe mental illness; 5. Those who have a history of drug abuse or alcohol abuse or need to drink a lot in the past 1 month; 6. Patients with drug allergy in this study; 7. Those who can't stop using the drugs or health products / foods that cause diarrhea and affect the intestinal flora in the test include western drugs or proprietary Chinese drugs, antibiotics, probiotic drug preparations, probiotic health products / foods, probiotic yoghurt, etc; 8. Those who have had colonoscopy (or intestinal cleansing treatment) in the past 1 month; 9. Pregnant or lactating women; 10. Those who are participating in or completing other clinical trials less than 3 months later; 11. Those who the researchers don't think are suitable for selection.

Design outcomes

Primary

MeasureTime frame
High throughput sequencing of feces;incidence of diarrhea;

Secondary

MeasureTime frame
gastrointestinal adverse reaction;

Countries

China

Contacts

Public ContactXin Lin

Suzhou Ninth People's Hospital

911283163@qq.com+86 18913720996

Outcome results

None listed

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