Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06524596
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-07-23
Brief Title:
Study on Gynecological Laparoscopy Under Total Intravenous Anesthesia
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Wuhan Childrens Hospital
Status:
COMPLETED
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 of preemptive analgesia with tartaric acid butorphanol on postoperative pain in gynecological laparoscopy under total intravenous anesthesia with remifentanilThis randomised double-blind placebo-controlled trial enrolled 60 patients undergoing elective gynaecological laparoscopy The patients were divided into two groups the butorphanol group n 30 and the control group n 29 Both groups received TIVA with propofol and remifentanil Observing two groups of patients on the visual analog scale the total consumption of rescue analogies and the confidence of postoperative nausea and vomiting PONV and the patient satisfaction score
Detailed Description:
To investigate the effect of preemptive analgesia with tartaric acid butorphanol on postoperative pain in gynecological laparoscopy under total intravenous anesthesia with remifentanilThis randomised double-blind placebo-controlled trial enrolled 60 patients undergoing elective gynaecological laparoscopy The patients were divided into two groups the butorphanol group n 30 who received 002 mgkg of tartaric acid butorphanol intravenously 30 minutes prior to anaesthesia induction and the control group n 29 who received the same volume of normal saline Both groups received TIVA with propofol and remifentanil The primary outcome was the visual analogue scale VAS score for pain at rest and on movement at 1 2 4 6 12 and 24 hours after surgery The secondary outcomes were the total consumption of rescue analgesics the incidence and severity of postoperative nausea and vomiting PONV and the patient satisfaction score
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