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Clinical Trials/NCT00623285
NCT00623285
Unknown
Phase 3

The Effects of Peri-operative Pregabalin Administration on Post-operative Analgesia in Patients Undergoing Coronary Bypass Grafting

University of Manitoba1 site in 1 country40 target enrollmentApril 2008

Overview

Phase
Phase 3
Intervention
Pregabalin
Conditions
Postoperative Pain.
Sponsor
University of Manitoba
Enrollment
40
Locations
1
Primary Endpoint
Pain scores and morphine consumption post surgery
Last Updated
15 years ago

Overview

Brief Summary

We hypothesize that the perioperative administration of pregabalin will significantly decrease pain scores and post-operative opioid requirements for patients undergoing coronary artery bypass grafting, and reduces the incidence of opioid-induced side effects such as respiratory depression. This may reduce ICU admission and possibly abbreviate length of hospital stay.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
June 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Group 1

Intervention: Pregabalin

Group 2

Intervention: Placebo/Lactose

Outcomes

Primary Outcomes

Pain scores and morphine consumption post surgery

Time Frame: 6 months

Secondary Outcomes

  • To determine the occurrence of opioid-related side effects such as nausea, vomiting, and respiratory depression in patients receiving pregabalin compared to those receiving placebo.(6 days)

Study Sites (1)

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