Effect of percutaneous acupoint stimulation during anesthesia resuscitation on perioperative recovery quality of patients undergoing gynecological laparoscopic surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200055338

Enrollment

Unknown

Registered

2022-01-07

Start date

2022-01-07

Completion date

Unknown

Last updated

2023-01-30

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

Conditions

None listed

Interventions

Transcutaneous Electrical Acupoint Stimulation Group:Transcutaneous Electrical Acupoint Stimulation

Control group:None

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are scheduled to undergo gynecological laparoscopic surgery; 2. ASA classification I-III; 3. Aged 18-65 years; 4. Education level above primary school; 5. Preoperative MMSE score >=23 points; 6. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Participated in other clinical trials within 4 weeks before surgery; 2. Severe heart, lung, liver, kidney and other organ dysfunction; 3. There is a history of neurological and psychiatric diseases, and a history of long-term use of sedative drugs; 4. Those with severe aphasia, visual and hearing impairment, and severe motor impairment who cannot cooperate with the examination; 5. Acupoint skin infection, damage, scarring; 6. Patients with preoperative sleep disorder.

Design outcomes

Primary

Measure	Time frame
Quality of recovery;Sleep quality;Postoperative pain score;	—

Secondary

Measure	Time frame
Waking quality;Postoperative cognitive function;Postoperative delirium;	—

Countries

China

Contacts

Public ContactYang Xiang

zzh3381090@qq.com+86 13087737227

Outcome results