Ignite Creation Date:
2024-05-06 @ 8:20 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06341270
Status:
RECRUITING
Last Update Posted:
2024-07-15
First Post:
2024-03-26
Brief Title:
Efficacy of TEAS on Postoperative Pain and Recovery in Patients Undergoing Hepatectomy
Sponsor:
West China Hospital
Organization:
West China Hospital
Study Overview
Official Title:
Efficacy of Transcutaneous Electrical Acupoint Stimulation on Postoperative Pain and Recovery in Patients Undergoing Hepatectomya Prospective Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to access the effect of transcutaneous electrical acupoint stimulation on postoperative pain in patients undergoing hepatectomy
Detailed Description:
Patients who meet the enrollment criteria will be randomized 11 to either the transcutaneous electrical acupoint stimulation TEASor the sham groups In the TEAS group the acupoints are bilateral neiguan PC6 HeguL14 YanglingquanGB34 ZusanliST 36 and RenyingST9 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 surgeryThe 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
Patients in the sham group will receive electrode attachment but without stimulation
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None