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Osteoarthritis clinical trials

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NCT ID: NCT04641546 Completed - Clinical trials for Osteoarthritis Shoulder

Effectiveness of Occupation-Based Intervention Compared With Therapeutic Exercise for Older Adults With Shoulder OA.

Start date: October 28, 2019
Phase: N/A
Study type: Interventional

As a registered and licensed occupational therapist, I completed a six-week evidence based research study to determine the effects of occupation-based intervention and therapeutic exercises versus therapeutic exercises alone.

NCT ID: NCT04640974 Completed - Clinical trials for Osteoarthritis, Ankle

Study of Cingal® for Symptomatic Relief of Osteoarthritis of Ankle Joint

Start date: January 14, 2021
Phase: N/A
Study type: Interventional

This Trial will obtain clinical data to support an expanded indication for a single injection of Cingal® used for the symptomatic relief of osteoarthritis in the ankle joint.

NCT ID: NCT04640961 Completed - Clinical trials for Osteoarthritis, Shoulder

Study of Cingal® for Symptomatic Relief of Osteoarthritis of Shoulder Joint

Start date: January 16, 2021
Phase: N/A
Study type: Interventional

This Trial will obtain clinical data to support an expanded indication for a single injection of Cingal used for the symptomatic relief of osteoarthritis in the shoulder joint.

NCT ID: NCT04640675 Not yet recruiting - Clinical trials for Osteoarthritis Pain of the Knee

A 12-week Study to Evaluate the Efficacy and Safety of HP-5000 in Subjects With Osteoarthritis Pain of the Knee

Start date: December 2020
Phase: Phase 3
Study type: Interventional

A 12-week, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase 3 study to Evaluate the Efficacy and Safety of HP-5000 in Subjects with Osteoarthritis (OA) Pain of the Knee

NCT ID: NCT04640298 Completed - Osteoarthritis, Hip Clinical Trials

Study of Cingal® for Symptomatic Relief of Osteoarthritis of Hip Joint

Start date: January 16, 2021
Phase: N/A
Study type: Interventional

This Trial will obtain clinical data to support an expanded indication for a single injection of Cingal used for the symptomatic relief of osteoarthritis in the hip joint.

NCT ID: NCT04638387 Terminated - Clinical trials for Osteoarthritis, Knee

PB125, Osteoarthritis, Pain, Mobility, and Energetics

Start date: November 3, 2020
Phase: N/A
Study type: Interventional

Nuclear factor erythroid 2-related factor 2 (Nrf2) is an important regulator in the body. It controls how well cells protect themselves against stress. PB125 (Pathways Bioscience) is a plant based activator of this important regulator Nrf2. PB125 is made up of three plant extracts (rosemary, ashwagandha, and Sophora japonica) so that it contains these things; 1. Carnosol, 2. Withaferin A, and 3. Luteolin. Carnosol comes from rosemary leaves. Rosemary is a spice often used in Italian foods and grown in many herb gardens all around Fort Collins. Withaferin A comes from the medicinal plant Withania somnifera, also called ashwagandha. Ashwaganda is commonly known as "Indian Winter cherry" or "Indian Ginseng" and it is one of the most important herbs of Ayurveda (the traditional system of medicine in India) used for millennia. Finally, luteolin is found widely in plants including those present in the diet (peppers, onions, celery, herbs/spices). Some people purchase these herbs commercially, and take them on their own for a variety of purposes. Typically, when you buy them, they will be in much higher doses than they are in PB125. What makes PB125 different is that very low doses of each of the 3 components work together-synergistically-to activate Nrf2 and increase the ability of cells to respond to stress. It is unknown if there are any benefits to taking PB125 and the risks are currently unknown. The purpose of this study is to examine changes in muscle, in joint pain, in mobility (standing and walking) and in leg strength that occur after consuming PB125 every day for 3 months. We want to make these measurements in people who have been diagnosed with mild to moderate osteoarthritis-a degenerative joint disease-in their knees.

NCT ID: NCT04637529 Completed - Osteoarthritis Clinical Trials

Efficacy and Safety of S (+) - Ibuprofen in Osteoarthritis Pain

APS003/2020
Start date: August 5, 2022
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of S (+) - ibuprofen compared to an active treatment for pain control in individuals diagnosed with osteoarthritis.

NCT ID: NCT04637490 Completed - Knee Osteoarthritis Clinical Trials

Patellar Resurfacing in Total Knee Arthroplasty Leads to Better Isokinetic Performance and Higher Clinical Scores

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

For decades there have been concerns about patellar resurfacing (PR) in total knee arthroplasty (TKA) and the individual preference of the surgeon is still the main determinant of whether or not resurfacing is applied. According to preference, surgeons can be categorized in 3 main groups of those who usually, selectively or rarely resurface. The aim of this prospective, randomized, controlled study to is compare the isokinetic performance and clinical outcome of TKAs with PR and without PR.

NCT ID: NCT04636229 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Efficacy of Amniotic Suspension Allograft in Patients With Osteoarthritis of the Knee

Start date: December 14, 2020
Phase: Phase 3
Study type: Interventional

This study is being conducted to evaluate the efficacy and safety of ASA compared to placebo in the management of osteoarthritis (OA) symptoms of the knee.

NCT ID: NCT04635176 Recruiting - Pain, Postoperative Clinical Trials

Comparing Local Anesthesia With and Without iPACK Block

Start date: October 30, 2022
Phase: Phase 4
Study type: Interventional

Total knee arthroplasty is an effective surgical intervention for patients with chronic osteoarthritis commonly performed worldwide. Postoperative pain management has been a key focus in patient care for this procedure. Poorly controlled pain following total knee arthroplasty is associated with decreased ambulation, increased length of hospital stay, increased complications (particularly related to significant opioid use), and overall suboptimal patient recovery. Appropriate postoperative pain management utilizing motor sparing peripheral nerve blocks and periarticular injections has been shown to provide faster, more optimized patient recovery and reduced hospital length of stay in patients undergoing total knee arthroplasty. Adductor canal block (ACB) is a well-studied peripheral nerve block performed for analgesia following total knee arthroplasty. ACB is an effective component of multimodal analgesia providing improved pain control to the peripatellar and intra-articular aspect of the knee joint while largely preserving the strength of the quadriceps muscles1. In addition, perioperative local infiltration analgesia (LIA) performed by the orthopaedic surgical team is a common practice that has been shown to improve short-term postoperative pain relief and reduce total systemic opioid consumption during hospital stay2 for total knee arthroplasty. The Infiltration between the Popliteal Artery and Capsule of the Knee (iPACK) block is a newly described regional anesthesia technique for postoperative analgesia in total knee arthroplasty, performed under ultrasound guidance. It targets the articular branches of the tibial, common peroneal, and obturator nerves in the popliteal region, and aims to provide analgesia to the posterior aspect of the knee joint without compromising lower extremity motor function following total knee arthroplasty. This study aims to determine whether the IPACK block provides additional analgesia (in combination with ACB + LIA) for total knee arthroplasty surgeries. The study will examine how much additional analgesia IPACK provides in the context of an already-optimized regional anesthesia pathway for total knee arthroplasty, which uses ACB + LIA, both modalities that have reasonable existing evidence.