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Knee Pain Chronic clinical trials

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NCT ID: NCT03334903 Completed - Knee Osteoarthritis Clinical Trials

Gabapentin Regimens and Their Effects on Opioid Consumption

Start date: May 15, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the best strategy of administering gabapentin in connection with our current approach to perioperative pain management. We aim to evaluate two different adjunct gabapentin regimens given in the perioperative period, and to identify which manages patient pain more effectively and safely. In this evaluation, we will identify the quantity of patients' opioid consumption, the quality of their pain management, and the frequency and severity of any side effects they might experience. Patients who are undergoing total knee replacement (TKR) and choose to participate will be randomly assigned to a treatment group using computer-generated randomization. Patients in group 1 (the control group) will receive the standard of care as pertains to gabapentin. This consists of a single 600 mg dose of gabapentin administered to the patient approximately one to two hours before surgery, then a dose of 600 mg each morning during postoperative admission. Patients in Group 2 will receive 600 mg preoperatively, plus an additional postoperative gabapentin regimen: they will take 300 mg of gabapentin every 8 hours for 1 week, then a single nightly dose of 300 mg for another month.

NCT ID: NCT03182686 Completed - Knee Osteoarthritis Clinical Trials

AP-003-C Study to Confirm the Efficacy of Ampion™ in Adults With Pain Due to Severe Osteoarthritis of the Knee

Start date: June 19, 2017
Phase: Phase 3
Study type: Interventional

This is a phase 3 randomized study to confirm the efficacy of an intra-articular injection of Ampion™ in adults with pain due to severe osteoarthritis of the knee.

NCT ID: NCT03112200 Completed - Osteoarthritis Clinical Trials

Subchondroplasty® Knee RCT

PRESERVE Knee
Start date: March 29, 2017
Phase: N/A
Study type: Interventional

This is a multi-center, prospective, single-blinded, two-arm study, randomized to include approximately 134 subjects treated with Subchondroplasty (SCP) + Arthroscopy and 67 subjects with arthroscopy alone. The primary objective of this study is to demonstrate superiority of Subchondroplasty with arthroscopy compared to arthroscopy alone for treatment of Bone Marrow Lesions (BMLs) in the knee.

NCT ID: NCT01345123 Completed - Back Pain Clinical Trials

Supporting Decision Making for Musculoskeletal Preference-Sensitive Care

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare condition oriented whole person Health Coaching along with the provision of decision aids to decision aids without condition oriented Health Coaching to neither condition oriented health coaching nor decision aids on medical cost, preference sensitive surgeries and measures of subject knowledge, decision process and decision quality.