Ignite Creation Date:
2024-10-25 @ 7:56 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06517069
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-18
Brief Title:
Effect of TEAS Combined With Oxycodone on Postoperative Visceral Pain in Gynecologic Laparoscopic Patients
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effect of Transcutaneous Electrical Acupoint Stimulation Combined With Oxycodone on Postoperative Visceral Pain and Early Recovery Quality in Gynecologic Laparoscopic Patients
Status:
RECRUITING
Status Verified Date:
2024-07
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:
To investigate the effect and feasibility of percutaneous acupoint stimulation combined with oxycodone on postoperative visceral pain in laparoscopic patients and provided a clinical basis for optimizing perioperative pain management in laparoscopic patients
Detailed Description:
Patients aged 18-65 years old BMI 18-30kgm2 ASA grade I or II were selected for gynecologic laparoscopic surgery laparoscopic ovarian tumor stripping laparoscopic uterine fibroid stripping laparoscopic total hysterectomy under general anesthesia from May 2024 to July 2024 Exclusion criteria Patients who were allergic to the drugs used in the study had confusion or cognitive impairment contraindicated percutaneous acupoint electrical stimulation abnormal cardiopulmonary and liver and kidney function history of analgesic drug use within one week history of diabetes myocardial infarction or cerebrovascular accident Exclusion criteria patients dropped out of the experiment midway or the data was not completely collected the surgical method changed midway the operation duration was less than 30 minutes or more than 2 hours and patients with opioid and addictive drug dependence
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