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Efficacy of TEAS on Postoperative Pain and Recovery in Patients Undergoing Hepatectomy

Liver Cancer Clinical Trial

Official title:
Efficacy of Transcutaneous Electrical Acupoint Stimulation on Postoperative Pain and Recovery in Patients Undergoing Hepatectomy：a Prospective, Randomized Controlled Trial

Clinical Trial Summary

The purpose of this study is to access the effect of transcutaneous electrical acupoint stimulation on postoperative pain in patients undergoing hepatectomy

Clinical Trial Description

Patients who meet the enrollment criteria will be randomized 1:1 to either the transcutaneous electrical acupoint stimulation (TEAS）or the sham groups. In the TEAS group, the acupoints are bilateral neiguan (PC6) , Hegu(L14), Yanglingquan(GB34), Zusanli(ST 36) and Renying(ST9) acupoints. Patients will receive TEAS 30min before anesthesia until being discharged from the post-anaesthesia care unit (PACU). The same treatment for 30 min will be performed on the 1st, 2nd and 3rd days after surgery.The stimulation intensity will be adjusted in accordance with the maximal level tolerated by each patient. Patients in the sham group will receive electrode attachment but without stimulation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06341270
Study type Interventional
Source West China Hospital
Contact Chunling Jiang, PhD
Phone 18980601096
Email jiang_chunling@yahoo.com
Status Not yet recruiting
Phase N/A
Start date April 20, 2024
Completion date December 20, 2026
View Details
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