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A for Postoperative Pain (NAPS Trial)

Phase 4
Waitlist Available
Led By Tuan Dinh, RPh
Research Sponsored by Hamilton Health Sciences Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Summary

The purpose of this study is to determine whether using an additional 48 hours of oral naproxen, after other post-operative pain medications have been stopped, will be effective in reducing opiate pain medication requirements and contribute to improved pain management.

Eligible Conditions
  • Postoperative Pain

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: AActive Control1 Intervention
Group II: PPlacebo Group1 Intervention

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Who is running the clinical trial?

Hamilton Health Sciences CorporationLead Sponsor
374 Previous Clinical Trials
340,012 Total Patients Enrolled
1 Trials studying Postoperative Pain
103 Patients Enrolled for Postoperative Pain
Tuan Dinh, RPhPrincipal InvestigatorSt. Joseph's Healthcare Hamilton
~1 spots leftby Sep 2025
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