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Protective effects and mechanisms of perioperative probiotic treatment on postoperative brain function injury in older patients undergoing non-cardiac surgery: a randomized, double-blind and placebo-controlled study

Protective effects and mechanisms of perioperative probiotic treatment on postoperative brain function injury in older patients undergoing non-cardiac surgery: a randomized, double-blind and placebo-controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045620
Enrollment
Unknown
Registered
2021-04-19
Start date
2021-03-16
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Postoperative Cognitive Dysfunction

Interventions

Control group:Placebo capsules

Sponsors

The Third Hospital of Xiangya
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients will have elective hip or knee replacement surgery; 2. Aged 60-90 years, regardless gender and race; 3. Without immune system disease; 4. Without psychiatric diseases and neurodegenerative diseases 5. Agree to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. The frequency of surgery is more than 1 times or need emergency surgery; 2. Preoperative coma, severe dementia, speech impairment, severe hearing or visual impairment, Parkinson's disease can not communicate; 3. Symptoms of intestinal obstruction or confirmed intestinal obstruction; requires a long time of total parenteral nutrition after surgery; 4. Antibiotics, probiotics, gastrointestinal motility drugs have been used within 10 days before admission; 5. With perioperative myocardial infarctions or cerebrovascular accidents 6. Postoperative hospital stay duration was less than 7 days 7. The attending physician or researcher believes there are other conditions that should not be included in this study.

Design outcomes

Primary

MeasureTime frame
Postoperative cognitive dysfunction;

Secondary

MeasureTime frame
The composition and change of fecal flora;Systemic inflammation level;

Countries

China

Contacts

Public ContactLe Yuan

Xiangya Medical College, Central South University

leyuanxy@csu.edu.cn+86 13787107617

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026