The effect of transcutaneous electrical acupoint stimulation on chronic pain after thoracoscopic surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100051841

Enrollment

Unknown

Registered

2021-10-07

Start date

2021-11-01

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

None listed

Interventions

TEAS group:TEAS for 30 min before anesthesia and after endotracheal extubation

Control group:None

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75; 2. American Society of Anesthesiologists (ASA) physical status of I–III; 3. Body mass index (BMI) 18-28 kg/m2; 4. Postoperative patient control intravenous analgesia.

Exclusion criteria

Exclusion criteria: 1. Contraindications to TEAS (scar or skin damage at the stimulation site, electronic devices such as pacemakers or other implanted medical electronic devices in the body); 2. Unable to communicate; 3. Long-term use of analgesics; 4. Receiving bilateral thoracoscopic surgery; 5. History of chest surgery; 6. History of chronic pain or neuropathic pain; 7. Autoimmune diseases and persistent infection; 8. Loss to follow-up.

Design outcomes

Primary

Measure	Time frame
NRS score;	—

Secondary

Measure	Time frame
Remifentanil consumption;The incidence of PONV;Demand for rescue analgesics;Neuropathic pain in patients;NRS score;The level of beta-endorphin in plasma of patients;The level of IL-6 in plasma of patients;	—

Countries

China

Contacts

Public ContactYi Lou

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicine

1254911509@qq.com+86 18930565679

Outcome results