CompletedPhase 4ketamine

Efficacy of Ketamine for Improvement in Postoperative Pain Control After Spinal Fusion for Idiopathic Scoliosis

Sponsored by Albany Medical College

NCT ID
NCT02651324
Target Enrollment
50 participants
Start Date
2013-05
Est. Completion
2017-12

About This Study

This study hypothesizes that the addition of a low-dose ketamine infusion to usual post-operative pain management will improve pain control as evidenced by an improvement in post-operative pain scores for patients undergoing spinal fusion for idiopathic scoliosis.

Conditions Studied

Idiopathic ScoliosisPost-operative Pain

Interventions

  • Ketamine
  • Placebo

Eligibility

Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* ASA I, II, III
* Presenting for spinal fusion for idiopathic scoliosis
* English-speaking and able to give assent

Exclusion Criteria:

* Any contraindication to ketamine
* Previous spinal surgery
* Opioid dependence
* Chronic pain condition
* Significant developmental delay
* Pregnancy

Study Locations (1)

Albany Medical Center
Albany, New York, United States

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source