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The Impact of Blood Transfusion-Induced Gut Microbiota Alteration on Cognitive Function: An observational study

The Impact of Blood Transfusion-Induced Gut Microbiota Alteration on Cognitive Function: An observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119598
Enrollment
Unknown
Registered
2026-02-28
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Postoperative cognitive dysfunction

Interventions

transfusion:None
control:None

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. age >= 18 years; 2. a patient in our hospital, to undergo elective surgery under general anaesthesia; 3. normal preoperative cognitive function; 4. patients and their families gave informed consent to participate in this study voluntarily and signed an informed consent form; 5. able to co-operate with the preoperative baseline survey, sample collection and postoperative cognitive function assessment and follow-up.

Exclusion criteria

Exclusion criteria: 1. preoperative history of cognitive dysfunction, dementia, or psychiatric illness; 2. preoperative presence of severe intestinal diseases or recent (within 3 months) use of antibiotics and other drugs that may affect intestinal flora; 3. Presence of serious perioperative complications such as severe infection, shock, and multi-organ failure; 4. a history of long-term alcohol consumption (=50g per day for more than 1 year) or substance abuse; 5. combination of severe hepatic and renal insufficiency, diabetic ketoacidosis, severe anaemia and other underlying diseases that may affect cognitive function or intestinal flora; 6. pregnant or lactating women; 7. those with an expected postoperative survival of less than 3 months, or those who are unable to complete the full follow-up.

Design outcomes

Primary

MeasureTime frame
gut microbiota;Postoperative cognitive dysfunction;

Secondary

MeasureTime frame
inflammation;

Countries

China

Contacts

Public ContactWEI XIN

The First Affiliated Hospital of Zhengzhou University

doctor_anwx@163.com+86 150 0399 5323

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026