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Randomized Controlled Trial Comparing Postoperative Pain Following TAH With GA vs. Combined GA + SAB

U

University of Saskatchewan

Status

Withdrawn

Conditions

Hysterectomy

Treatments

Drug: General Anesthesia (control group)
Drug: General Anesthesia + Spinal anesthesia combined

Study type

Interventional

Funder types

Other

Identifiers

NCT01511627
RCT GA + SAB for TAH

Details and patient eligibility

About

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.

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

General Anesthesia
Active Comparator group
Treatment:
Drug: General Anesthesia (control group)
General Anesthesia + Spinal Anesthesia
Experimental group
Treatment:
Drug: General Anesthesia + Spinal anesthesia combined

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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