Clinical Trials Directory

Trials / Completed

CompletedNCT00738192

Comparison of Analgesic Efficacy of Fentanyl, Sufentanil and Butorphanol After Remifentanil Anesthesia

Comparison of Analgesic Efficacy of Fentanyl, Sufentanil and Butorphanol After Remifentanil Anesthesia in Gynecological Laparoscopic Surgeries

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Nanjing Medical University · Academic / Other
Sex
Female
Age
19 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Fast awakening from anesthesia is one of the major characteristics of remifentanil-associated anesthetic induction and maintenance, whereas corresponding pain during awakening influences patient's rehabilitation strongly. In addition, such early postoperative pain results in significant stress responses, which displays as further release of stress hormones such as cortisol and β-endorphin as well. How to prevent such acute pain resulting from remifentanil's fast metabolism endows clinical significance. This study is designed to compare the analgesic efficacy of fentanyl, sufentanil and butorphanol delivered after gynecological laparoscopic surgeries that underwent remifentanil induction and maintenance, and investigate corresponding influence on the levels of blood cortisol and β-endorphin.

Conditions

Interventions

TypeNameDescription
DRUGFentanyl citrateFentanyl 0.5 μg/kg delivered intravenously immediate at the end of remifentanil pump finished
DRUGSufentanil citrateSufentanil 0.05 μg/kg delivered intravenously immediate at the end of remifentanil pump finished
DRUGButorphanol tartrateButorphanol 0.01 mg/kg delivered intravenously immediate at the end of remifentanil pump finished

Timeline

Start date
2008-07-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2008-08-20
Last updated
2009-03-11

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00738192. Inclusion in this directory is not an endorsement.