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Phase 4 Completed N=50 Randomized Triple-blind Treatment

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

Idiopathic Scoliosis · Post-operative Pain
Source: ClinicalTrials.gov NCT02651324 ↗
Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Feb 2025
Primary outcomePrimary: Patient Satisfaction — 2.75; 2.92; 3.31; 3.13 score on a scale
◆ Published Evidence
No publication linked

No peer-reviewed publication reporting this trial's results has been linked yet. This can indicate results are unpublished — a known publication-bias signal. We re-check periodically.

Summary

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Patient Satisfaction
2.75; 2.92; 3.31; 3.13
SECONDARY
Pain Score
3.17; 3.9
SECONDARY
Opioid Use
0.577; 0.83
SECONDARY
Length of Stay
5.46; 5.52

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02651324). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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