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Alteration of the gut microbiota and degree of gastric and small intestine mucous injury before and after 6 months of dual antiplatelet therapy

Alteration of the gut microbiota and degree of gastric and small intestine mucous injury during dual antiplatelet therapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016425
Enrollment
Unknown
Registered
2018-06-01
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-06-05

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

Conditions

small intestine injury

Interventions

Case series:dual antiplatelet therapy

Sponsors

Beijing Anzhen Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. subjects with the age between 18 and 80 years; 2. subjects diagnosed as stable angina pectoris; 3. subjects who plan to use dual antiplatelet drugs after PCI at least June mouths; 4. subjects who agree to receive research treatment; 5. All subjects are voluntary and sign informed agreement.

Exclusion criteria

Exclusion criteria: 1. subjects receiving relevant drugs that have an impact on the experimental results in recent one month, the relevant drugs include: (1) antibiotics; (2) probiotics; (3) various drugs that inhibit gastric acid secretion (proton pump inhibitors and H2 receptor antagonists, etc.); (4) cytokines, immunosuppressants and cytotoxic agents; (5) hormones; (6) other drugs that affect the stomach biota. 2. subjects with capsule endoscopy for contraindications, including suspected or known gastrointestinal obstruction, stenosis, fistula, or diverticulum, a pregnant woman, a previous surgical operation of the digestive tract, or a change in the structure of the abdominal digestive tract, or refusing to accept any abdominal surgery (Once the capsule is in detention, it may need to be removed by surgery). 3. subjects taking other antiplatelet drugs or anticoagulant drugs at the same time; 4. PPI, mucosal protectant or other acid suppressant can not be restricted according to the regulations; 5. subjects diagnosed as acute coronary syndromes; 6. subjects with a history of peptic ulcers or hemorrhagic diseases; 7. peptic ulcer or gastrointestinal tumor was diagnosed by capsule endoscopy; 8. subjects who were allergic to aspirin, clopidogrel and polyethylene glycol electrolyte dispersion.

Design outcomes

Primary

MeasureTime frame
gut microbiota;degree of small intestine mucous injury;Inflammatory factors;degree of gastric mucous injury;

Secondary

MeasureTime frame
Medical history;Combined use of drugs;

Countries

China

Contacts

Public ContactZhang Jie

Beijing Anzhen Hospital, Capital Medical University

zhangjie4155@sina.com+86 13601337670

Outcome results

None listed

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