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Clinical study on the improvement of perioperative neurocognitive disorders in elderly patients undergoing gastrointestinal surgery by Tongdu Yangshen Acupuncture

Clinical study on the improvement of perioperative neurocognitive disorders in elderly patients undergoing gastrointestinal surgery by Tongdu Yangshen Acupuncture

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068102
Enrollment
Unknown
Registered
2023-02-07
Start date
2023-02-08
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

perioperative neurocognitive disorders

Interventions

Control group:N/A
Electric acupuncture group:Tongdu Yangshen Acupuncture

Sponsors

Guangdong Provincial Hospital of Chinese Medicine(The Second Affiliated Hospital of Guangzhou University of Chinese Medicine)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients who plan to receive gastrointestinal tumor surgery under endotracheal intubation and general anesthesia; 2. ASA grade ?~?, surgery grade 3~4; 3. Aged 65-85 years; 4. Volunteer to participate in research projects.

Exclusion criteria

Exclusion criteria: 1. Patients with central nervous system or mental diseases; 2. Patients with cognitive dysfunction before surgery; 3. Patients whose operation time is expected to exceed 2.5 hours; 4. Long-term preoperative use of sedatives, antidepressants, NSAIDs (non-steroidal anti-inflammatory drugs) and hormones; 5. Alcoholics and drug addicts; 6. Severe disorder of internal environment and insufficiency of heart, lung, liver and kidney function; 7. Severe visual or hearing impairment or inability to communicate; 8. Those who have systematically received nootropics from Chinese and Western medicine in the past two weeks; 9. Patients who participated in other clinical trials 3 months before study inclusion; 10. Patients with known drug or liquid allergy.

Design outcomes

Primary

MeasureTime frame
Incidence of perioperative cognitive dysfunction (cognitive function score);

Secondary

MeasureTime frame
Incidence of hypotension during anesthesia induction;Intraoperative cerebral oxygen saturation;Intraoperative vital signs;Vascular drug dosage in operation center;Intraoperative hemodynamics;Intraoperative lactic acid value;Postoperative stay in ICU and total postoperative hospitalization;

Countries

China

Contacts

Public ContactDeng Jinhe

Guangdong Provincial Hospital of Chinese Medicine(The Second Affiliated Hospital of Guangzhou University of Chinese Medicine)

djh13751803925@163.com+86 137 5180 3925

Outcome results

None listed

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