Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The Opioid-Sparing Protocol (OSP) is a multimodal analgesic regimen developed by Taipei Veterans General Hospital for managing postoperative pain in patients undergoing simultaneous bilateral total knee arthroplasty (TKA). The protocol is designed to provide effective pain control while minimizing the requirement for systemic opioids and reducing opioid-related complications. It consists of a combination of pharmacological agents and regional anesthesia techniques, including intravenous parecoxib (a selective COX-2 inhibitor), ultrasound-guided adductor canal blocks and periarticular injections using bupivacaine, and postoperative oral administration of celecoxib and paracetamol. In a Phase 4 clinical trial (NCT04314505), the OSP demonstrated equivalent analgesic efficacy to traditional morphine-based patient-controlled analgesia (PCA) while significantly decreasing total morphine consumption in the immediate postoperative period.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Opioid-Sparing Protocol.