Clinical Trials Directory

Trials / Completed

CompletedNCT00795314

Propofol-butorphanol Anesthesia During Uterine Curettage

Propofol-butorphanol Combined Anesthesia During Uterine Curettage on Abortion

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

Uterine curettage is usually performed under the anesthesia of propofol-fentanyl or para-cervical block,of which generally has significant incidence of respiratory depression which increases the demand on intraoperative monitoring, or has unavoidable insufficient blockade which results in intraoperative suffering of pain. Butorphanol is an analgesic with combined effects on mu and kappa opioid receptors leading to a role as analgesia and sedation. The investigators hypothesized that combined propofol with butorphanol during uterine curettage would produce optimal effectiveness of these two drugs by adding sedative and analgesic effects together. In addition, it would decrease the intraoperative consumption of propofol without increase the incidence of side effects. Furthermore, such combination would alleviate postoperative pain.

Conditions

Interventions

TypeNameDescription
DRUGFentanyl CitrateCombined anesthesia with propofol (2-2.5mg/kg) and fentanyl (5 μg)
DRUGButorphanol TartrateCombined anesthesia with propofol (2-2.5 mg/kg) and butorphanol (1mg)

Timeline

Start date
2008-11-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2008-11-21
Last updated
2009-07-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00795314. Inclusion in this directory is not an endorsement.