Ignite Creation Date:
2024-10-25 @ 7:53 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06541561
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-02
Brief Title:
Efficacy of TEAS on Postoperative Pain and Recovery in Patients Undergoing Pancreatectomy
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Efficacy of Transcutaneous Electrical Acupoint Stimulation on Postoperative Pain and Recovery in Patients Undergoing Pancreatectomy a Prospective Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
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 pancreatectomy
Detailed Description:
Patients who meet the enrollment criteria will be randomized 11 to either the transcutaneous electrical acupoint stimulation TEAS or the sham groups In the TEAS group the acupoints are bilateral neiguan PC6 and Zusanli ST 36 acupoints Patients will receive TEAS 30min before anesthesia until being discharged from the postanaesthesia 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
Patients in the sham group will receive electrode attachment but without stimulation
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None