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Clinical Trials/NCT00733564
NCT00733564
Completed
Not Applicable

Evaluation of the Anesthetic Efficacy of Propofol,Sevoflurane and Paracervical Block for Uterine Curettage

Nanjing Medical University1 site in 1 country150 target enrollmentAugust 2008

Overview

Phase
Not Applicable
Intervention
Lidocaine
Conditions
Uterine Curettage
Sponsor
Nanjing Medical University
Enrollment
150
Locations
1
Primary Endpoint
Bispectral Index (BIS) value
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

Anesthesia during uterine curettage is a problem. Paracervical block is used in general for such an operation, though, the anesthetic efficacy is incomplete. Propofol is the short-lasting intravenous anesthetic administrated popularly. Sevoflurane is a new inhalational anesthetic well-known for it's "easy come, easy go" property. The investigators hypothesized that propofol, sevoflurane and paracervical block had different anesthetic efficacy during uterine curettage. Which one is the optimal selection for such operation needed to be evaluated.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
March 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Nanjing Medical University

Eligibility Criteria

Inclusion Criteria

  • ASA status I-II
  • Performing abortion operation (medical- or surgical)
  • Requiring painless abortion

Exclusion Criteria

  • \< 19 yrs, and \>=45 yrs
  • History of central active drugs administration
  • Drug abuse
  • Hypertension
  • Any other chronic diseases
  • Allergy to the study drugs
  • Habit of over-volume alcohol drinking
  • Records of history of centrally active drug use and psychiatry
  • Any organic disorder

Arms & Interventions

1

Paracervical block will be performed

Intervention: Lidocaine

2

Propofol anesthesia will be performed

Intervention: Propofol

3

Sevoflurane anesthesia will be performed

Intervention: Sevoflurane

Outcomes

Primary Outcomes

Bispectral Index (BIS) value

Time Frame: 0, 5, 10, 20, 30min after anesthesia

Secondary Outcomes

  • Pain intensity(0, 5, 10, 20, 30min after surgical procedures)
  • Arterial blood gas analysis(5min before operation; 1min and 5min after beginning of the operation)
  • Cortisol level(30min before operation; 1 and 5min during operation)
  • Intraoperative awareness(0, 5, 10, 20, 30min after anesthesia)
  • Vital signs(0, 5, 10, 15, 20, 25, 30min after anesthesia)
  • Uterine bleeding(0min after completion of the operation; 1 hour after the operation)
  • Side effects(30min after operation)

Study Sites (1)

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