🏛️ Verified NIH Record • Updated 2019-05-07
Tramadol Versus Placebo and Morphine in the Management of Post-Operative Pain Abdominoplasty (NCT03774836)
A Phase 3, Multicenter, Randomized, Double-Blind, Three-Arm Study to Evaluate the Efficacy and Safety of Tramadol Infusion (AVE-901) Versus Placebo and Morphine in the Management of Postoperative Pain Following Abdominoplasty
🔵 Active, Not Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Avenue Therapeutics, Inc.
🩺 Plain-English Summary (8th-Grade Level)
This study is evaluating the analgesic efficacy of intravenous (IV) tramadol (AVE-901) compared to placebo in the management of postoperative pain following abdominal surgery.
Who can join: Review the eligibility criteria below.
Location: Lotus Clinical Research — Pasadena, California
Age range: 18 Years to 75 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (3 Sites)
- Lotus Clinical Research — Pasadena, California
- Hermann Drive Research — Houston, Texas
- Endeavor Clinical Trials — San Antonio, Texas
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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Explore by condition: All Pain Management clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.