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Reconstructing the dysbiosis intestinal environment cohort study

Reconstructing the dysbiosis intestinal environment cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105470
Enrollment
Unknown
Registered
2025-07-03
Start date
2025-07-07
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Intestinal flora

Interventions

FMT Group:FMT capsule delivery
Bifidobacterium Triplex Capsules:Bifidobacterium triplex capsule administration

Sponsors

Shenzhen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. 18-65 years old patients with dysbiosis (based on the results of drug sensitivity testing in our hospital or a tertiary hospital); 2. patients with dysbiosis should meet one of the following conditions: (1) the patient's clinical symptoms of refractory diarrhea; (2) the patient is not effective in the treatment of existing means of treatment or the effect is not obvious (the effect is defined as the continuation of diarrhea after the use of the drug); (3) able to be administered through the jejunum tube; 3. The subject and family members ( or guardians) fully read, understood and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.patients with extremely severe disease and expected to die within 48 hours; 2. patients with non-intestinal dysbiosis; 3. patients with severe dysbiosis and gastrointestinal bleeding;

Design outcomes

Primary

MeasureTime frame
Effectiveness in curing diarrhea symptoms;

Secondary

MeasureTime frame
Inflammatory indicators;Immunity indicators;

Countries

China

Contacts

Public ContactLiu Xueyan

Shenzhen People's Hospital

13554843721@163.com+86 180 2538 8894

Outcome results

None listed

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