Safety of Buprenorphine Transdermal System (BTDS) in Subjects With Acute Postoperative Pain After Total Knee Replacement
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Pilot Study to Evaluate the Analgesic Efficacy of BTDS on Postoperative Pain During Rehabilitation Following Total Knee Arthroplasty
Sponsor: Purdue Pharma LP
Terminated
due to administrative reasons not related to efficacy or safety.
Other terminated trials from Purdue Pharma LP
- Attention Deficit/Hyperactivity Disorder · Phase PHASE4 · Apr 2022
- Attention-Deficit/Hyperactivity Disorder · Phase PHASE4 · Jan 2022
- Osteoarthritis Pain of the Knee · Phase PHASE2 · Nov 2016
- Postsurgical Pain Due to Third Molar Extraction · Phase PHASE2 · Nov 2013
- Back Pain Lower Back Chronic · Phase PHASE3 · Jan 2008
Other Postoperative Pain trials with similar outcome
A PHASE2 clinical study on Postoperative Pain, this trial is terminated or withdrawn. The trial is conducted by Purdue Pharma LP and has accumulated 7 data snapshots since 2006. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
7 versions recorded-
Sep 2024 — Present [monthly]
Terminated PHASE2
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE2
-
Dec 2021 — Jul 2024 [monthly]
Terminated PHASE2
-
Jan 2021 — Dec 2021 [monthly]
Terminated PHASE2
-
Jun 2018 — Jan 2021 [monthly]
Terminated PHASE2
▶ Show 2 earlier versions
-
Feb 2017 — Jun 2018 [monthly]
Terminated PHASE2
-
Jan 2017 — Feb 2017 [monthly]
Terminated PHASE2
First recorded
Nov 2006
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Purdue Pharma LP
For direct contact, visit the study record on ClinicalTrials.gov .