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Gut microbiota and delirium in old patients given propofol or sevoflurane anaesthesia for total knee arthroplasty

Gut microbiota and delirium in old patients given propofol or sevoflurane anaesthesia for total knee arthroplasty

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087263
Enrollment
Unknown
Registered
2024-07-23
Start date
2023-05-31
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Postoperative delirium

Interventions

Sevoflurane group:Patients were inhaled with 2%-5% sevoflurane and received remifentanil 6-12ug/kg/h intravenously to maintain anesthesia
Propofol group:Patients received propofol 4-12mg/kg/h and remifentanil 6-12ug/kg/h intravenously to maintain anesthesia

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
65 Years to 86 Years

Inclusion criteria

Inclusion criteria: 1. The patients who received total knee arthroplasty; 2. Patients aged over 65 years; 3. Female; 4. Patients with ASA classification II-III 5. BMI (Body mass index) : 18.5-27.9kg/m2; 6. Patients who scheduled for the first surgery of the day; 7. Patients and their family members who have written consent before enrolment.

Exclusion criteria

Exclusion criteria: 1. Those who have severe hypertension and untreated before operation, history of diabetes, Cardiovascular and cerebrovascular diseases, endocrine system diseases, hyperlipidemia; 2. Patients with severe hepatic and renal insufficiency; 3. Those who have a history of gastrointestinal tract surgery before operation, and those with inflammatory bowel disease and functional dyspepsia; 4. Those who have a history of chemotherapy, radiation exposure; 5. Individuals who have recently (within 6 months) received antibiotics or hormone medications; 6.Patients with neuropsychiatric diseases or anxiety, recent or long-term use of sychotropic drug; 7. Those with a score of = 1 on 4AT; 8. Patients with sleep disorders; 9. Patients who have used anticholinergic drugs during surgery; 10. Patients with blood loss >300ml; 11. Receiving surgical patients; 12.Those who refused to participate in the experiment.

Design outcomes

Primary

MeasureTime frame
The alpha diversity index of intestinal flora (Shannon index);The alpha diversity index of intestinal flora (Simpson index);The alpha diversity index of intestinal flora (ACE index);The alpha diversity index of intestinal flora (Chao1 index);the relative abundance of intestinal flora at phylum level (Firmicutes);the relative abundance of intestinal flora at phylum level (Bacteroidetes);the relative abundance of intestinal flora at phylum level (Actinobacteria);the relative abundance of intestinal flora at phylum level (Proteobacteria);postoperative delirium;

Secondary

MeasureTime frame
VAS scores;First anal exhaust time and defecation time;

Countries

China

Contacts

Public ContactYANG Kun

First Affiliated Hospital of Kunming Medical University

ykun74@aliyun.com+86 137 0060 2170

Outcome results

None listed

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