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TEAS improves postoperative sleep disorders in olderly patients undergoing laparoscopic surgery by regulating intestinal microbiota: a prospective, randomized, controlled study

TEAS improves postoperative sleep disorders in olderly patients undergoing laparoscopic surgery by regulating intestinal microbiota: a prospective, randomized, controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086911
Enrollment
Unknown
Registered
2024-07-15
Start date
2023-10-23
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

urologic tumor

Interventions

TEAS dexmedetomidine group:TEAS stimulation and using dexmedetomidine
TEAS saline group:only apply TEAS stimulation
sham dexmedetomidine group:sham stimulation and using dexmedetomidine
sham saline group:only apply sham stimulation

Sponsors

Beijing Friendship Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: ? Age >60 years, not limited to gender; ? ASA grade: I-II; ? Patients undergoing elective urologic laparoscopic surgery; ? Patients had preoperative sleep disorders; ? Body mass index (BMI): 18 kg/m^2 1h; ? Hospitalization time >2 days; ? The Pittsburgh Sleep Quality Index (PSQI) scale was used to successfully assess the patient's sleep in the last month 24h before surgery; ? Surgeries are performed by the same surgical team; ? Voluntarily participated in the trial and signed the informed consent form

Exclusion criteria

Exclusion criteria: ? Surgical incisions or scarring in the meridian where the acupuncture point is located; ? Infection of the skin around the acupuncture point; ? Having nerve damage to the upper or lower extremities; ? A history of alcoholism or drug dependence; ? Combined cardiovascular, nerve, brain or mental disease; ? Long-term use of analgesic drugs; ? Having obstructive sleep apnea-hypopnea syndrome; ? Having a history of abdominal surgery or recovery from anesthesia; ? Patients with psychological disorders or verbal communication difficulties; ? Intended to be transferred to ICU after surgery.

Design outcomes

Primary

MeasureTime frame
Pittsburgh sleep quality index;Athens insomnia scale;Objective postoperative assessment of sleep quality;

Secondary

MeasureTime frame
Postoperative VAS scores;Changes in the perioperative intestinal microbiota;Dosage of postoperative analgesic and anesthetic medications;Intraoperative vital signs;length of surgery;length of anesthesia;length of extubation;Changes in the perioperative brain-gut peptides;postoperative complications;length of hospitalization;hospitalization costs;

Countries

China

Contacts

Public ContactLi Zhang

Beijing Friendship Hospital Affiliated to Capital Medical University

zhangli8828@163.com+86 139 1182 2346

Outcome results

None listed

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