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Clinical Trials/NCT01511627
NCT01511627
Withdrawn
Not Applicable

A Randomized Controlled Trial Comparing Postoperative Pain Following Total Abdominal Hysterectomy With General Anesthetic vs. Combined General and Spinal Anesthetic

University of Saskatchewan1 site in 1 countryJanuary 2012

Overview

Phase
Not Applicable
Intervention
General Anesthesia (control group)
Conditions
Hysterectomy
Sponsor
University of Saskatchewan
Locations
1
Primary Endpoint
Total Morphine consumption
Status
Withdrawn
Last Updated
9 years ago

Overview

Brief Summary

The investigators hypothesize that a spinal anesthetic administered prior to the induction of general anesthesia will result in reduced need for pain medication and reduced postoperative pain, as well as reduced hospital stay following a total abdominal hysterectomy.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
July 2012
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jacelyn Larson

Faculty

University of Saskatchewan

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists' (ASA) I and II patients undergoing elective Total Abdominal Hysterectomy at the Saskatoon City Hospital
  • Lower transverse abdominal incision

Exclusion Criteria

  • BMI \> 40
  • The TAH is treatment for cancer
  • A history of regular opioid use
  • Any medical condition that would make a spinal inadvisable,
  • An allergy or medical condition that would make it inadvisable to receive the drugs used in this study (eg. Peptic ulcer disease), or
  • If you will also be having a salpingo-oophorectomy).

Arms & Interventions

General Anesthesia

Intervention: General Anesthesia (control group)

General Anesthesia + Spinal Anesthesia

Intervention: General Anesthesia + Spinal anesthesia combined

Outcomes

Primary Outcomes

Total Morphine consumption

Time Frame: Post-operative day 2

The primary outcome will be total opioid use per day, as recorded by the PCA pump and transcribed by the nursing staff in the PACU and on the post-operative ward.

Morphine consumption

Time Frame: 1 day

The primary outcome will be total opioid use per day, as recorded by the PCA pump and transcribed by the nursing staff in the PACU and on the post-operative ward.

Secondary Outcomes

  • Pain score on the VAS(On post-operative day 2 at 22:00)

Study Sites (1)

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