Skip to content

A Study on the Application Effect of Perioperative Electroacupuncture Therapy in Promoting Rapid Recovery after Spinal Endoscopic Surgery under General Anesthesia

A Study on the Application Effect of Perioperative Electroacupuncture Therapy in Promoting Rapid Recovery after Spinal Endoscopic Surgery under General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000549
Enrollment
Unknown
Registered
2024-10-14
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Acute postoperative pain

Interventions

Control group:Intravenous suctioning compound general anesthesia
Experimental group:Electroacupuncture combined with intravenous aspiration combined with general anesthesia

Sponsors

Guangzhou Hospital of Traditional Chinese Medicine Affiliated to Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Initial spinal endoscopic surgery; (2) Gender is not limited age = 18 years old; (3) United States Society of Anesthesiologists ASA grade I-III; (4) The intraoperative anesthesia method is tracheal intubation and general anesthesia; (5) Able to understand NRS score anxiety scale depression scale and pain catastrophizing scale; (6) Voluntary participation patients or family members sign the informed consent form and include patients in clinical ethics treatment.

Exclusion criteria

Exclusion criteria: (1) Patient does not agree to participate in the study or surgery and has not signed the informed consent form; (2) Have severe cardiovascular system diseases or chronic respiratory diseases such as COPD etc.; (3) Those with a history of stroke or transient ischemic attack; (4) history of hypersensitivity to analgesic drugs used in this study; (5) Have a history of drug addiction; (6) Are taking antidepressants or sedatives etc.; (7) Have central nervous system diseases.

Design outcomes

Primary

MeasureTime frame
Pain catastrophizing scale score;

Secondary

MeasureTime frame
Quality of life scores;Depression Scale;Diagnose APSP;Anxiety scales;

Countries

China

Contacts

Public ContactLuyi

Guangzhou Hospital of Traditional Chinese Medicine Affiliated to Guangzhou Medical University

louis0731@qq.com13826495169

Outcome results

None listed

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