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Clinical Trial Summary

The primary objective of this study is to determine if gabapentin can decrease or prevent chronic post-thoracotomy pain.


Clinical Trial Description

This study is a prospective double blind randomized controlled trial evaluating the peri-operative use of gabapentin in the prevention or modulation of post-thoracotomy hyperalgesia. Treatment will consist of a 600 mg dose of gabapentin or placebo given preoperatively the night before surgery, based on a computer generated randomized assignment. The treatment group will continue to be medicated with gabapentin 300 mg twice daily for one month following surgery. Those not included in the treatment arm of the study will continue to take a placebo for the same duration. Follow-up will consist of a postoperative visit at approximately 48 hours and a one month clinical visit. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00934193
Study type Interventional
Source University of Kansas Medical Center
Contact
Status Withdrawn
Phase Phase 3
Start date July 2009
Completion date June 2011

See also
  Status Clinical Trial Phase
Completed NCT01726205 - Perioperative Pregabalin and Continuous Wound Infusion for Pain Control Following Thoracotomy Phase 4
Completed NCT03618225 - Duloxetine Role in Reducing Opioid Consumption After Thoracotomy Phase 4