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Joint Diseases clinical trials

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NCT ID: NCT03647709 Completed - Clinical trials for Arthropathy of Knee Joint

Opioid-free Accelerated Recovery Total Knee Arthroplasty

Start date: October 1, 2018
Phase:
Study type: Observational

To prove that total knee arthroplasty can be performed with little, if any need for opioids by using a combination of patient education, optimized pre-op and post-op pain and recovery protocols. The goal being opioid-free total knee arthroplasty.

NCT ID: NCT03639532 Completed - Osteoarthritis, Hip Clinical Trials

Ceramic-on-Ceramic Versus Ceramic-on-HXLPE THA

Start date: January 1, 2000
Phase: Phase 4
Study type: Interventional

Methods to reduce the revision rate of total hip arthroplasties (THAs) because of wear-related issues are important to examine, particularly because younger patients have a disproportionately high risk of revision. The investigators hoped to follow up patients and see if long-term Harris hip scores and WOMAC scores better in younger patients with a ceramic-on-ceramic (COC) THA compared with those with a ceramic-on-highly-cross-linked polyethylene (COP) THA.

NCT ID: NCT03632707 Completed - Clinical trials for Medial Meniscus, Posterior Horn Derangement

Magnetic Resonance Imaging of Medial Meniscal Posterior Root Tear

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate and analyze the role of magnetic resonance imaging in the diagnosis of medial meniscal posterior root tears, including the normal variations in meniscal anatomy that may resemble a meniscal tear, and identifying the causes or nature of posterior medial meniscal root tear(degenerative versus traumatic) and correlate the results with the standard reference knee Arthroscopy.In addition to identifying and estimating the suspected cases of meniscal extrusion by making MRI with stress varus overloading simulating weight bearing.

NCT ID: NCT03622684 Completed - Clinical trials for TEMPOROMANDIBULAR JOINT DYSFUNCTION SYNDROME

Progressive Muscle Relaxation According to Jacobson in Treatment of the Patients With Temporomandibular Joint Disorders

Start date: March 20, 2014
Phase: N/A
Study type: Interventional

Temporomandibular joint disorders are ranked third among the most common stomatological diseases after dental caries and periodontal problems. Type of dysfunction is determined by environmental, genetic and psycho-emotional factors. It has been observed that increasing level of stress leads to the increase of harmful parafunctional habits in the stomatognathic system whose long-term effect prevents the ability of the organism to compensate and adapt the function, which contributes to the pain within the masticatory system. Nowadays applied methods in treatment of temporomandibular joint disorders are still under investigation. However, they have not been developed effectively yet. Satisfactory methods of masticatory muscle relaxation (with the exception for drug treatment) are only related to mental patients. Significant impact factor and psycho-emotional stress in the etiology of dysfunction indicate the need of the routine approach in the treatment of patients with temporomandibular joint disorders to be changed. The attempt to cooperate with a psychologist may facilitate the effectiveness of traditional rehabilitation of patients with dysfunction.

NCT ID: NCT03617107 Active, not recruiting - Rotator Cuff Tear Clinical Trials

Reverse Total Shoulder Arthroplasty: A Data Analysis on Patients Undergoing Reverse Total Shoulder Arthroplasty

rTSA
Start date: December 15, 2017
Phase:
Study type: Observational

The purpose of this study is to evaluate reverse total shoulder arthroplasty patients preoperative objective measurements and operative objective measurements to determine if there is any effect to postoperative outcomes. Patients who were 18 years old or greater at the time of surgery were followed clinically and radiographically to determine best practice and optimal treatment and technique, risk and rate of complication, and postoperative outcomes.

NCT ID: NCT03616340 Not yet recruiting - Rotator Cuff Tear Clinical Trials

Efficacy of Intra-articular NSAID Versus Corticosteroid in the Treatment of Shoulder and Knee Conditions: A Randomized, Double-Blind, Prospective Study

Start date: August 2018
Phase: Phase 3
Study type: Interventional

The proposed study will compare the efficacy of Triamcinolone versus Ketorolac for intra-articular injection of the knee and shoulder

NCT ID: NCT03605290 Completed - Surgery Clinical Trials

Comparison Between Two Operational Techniques for Total Knee Replacement

Start date: June 15, 2018
Phase: N/A
Study type: Interventional

Advance Knee osteoarthritis is treated by Total knee replacement. Since the first TKR in 1973 there has been continuous advance in implant technology as well as operative technique, yet current patient satisfaction after the procedure is accepted to be about 80%. There are a few operative techniques to perform TKR. Until recently the most common technique is the anterior approach to the knee and then using mechanical instrumentation to make the bone cuts for the femur and tibia. A second popular technique is the anterior approach to the knee and then using a kinematic alignment to make the bone cuts. The investigators wish to compare short term results of the two operative techniques as evidenced in patient objective functional scores and also by evaluating the gait of the patients by using the REHAGAIT ANALYZER PRO by HASOMED inc. Magdeburg Germany.

NCT ID: NCT03601728 Suspended - Clinical trials for Arthropathy of Knee Joint

A Personalized Prehabilitation Intervention In Elective Joint Replacement Surgery

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

The mission is to develop novel interventions to improve cognitive function, and thereby reducing delirium in hospitalized patients to improve perioperative outcomes. Delirium affects up to 42% of hospitalized patients and disproportionately increases morbidity and mortality in older adults, especially after surgical procedures. Current approaches prevent only 30-40% of delirium cases. The goal is to use prehabilitation (an individualized exercise regimen performed in the 2-4 weeks prior to admission) to improve peri-operative cognitive status, mobility and recovery. Based on preliminary data, the investigators propose to deeply phenotype patients, meaning to study the patient, the disease and surgery in a very detailed fashion, with elective knee or hip replacement surgery and use a personalized prehabilitation intervention compared to standard pre-operative care. To facilitate data collection over the course of the study, the investigators use wearable devices and mobile phone applications.

NCT ID: NCT03599336 Terminated - Arthropathy Clinical Trials

RSA vs. Nonop for 3 & 4-Part Proximal Humerus Fractures

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

There is currently no consensus amongst orthopedic specialists on the best way to treat 3- and 4-part proximal humerus fractures. No surgery and surgery with a type of shoulder replacement called a reverse total shoulder arthroplasty are two options that many orthopedists use. This study is being performed to evaluate the differences in short- and long-term pain and functional outcomes between patients who are treated with these two different options.

NCT ID: NCT03599024 Completed - Hip Joint Disorders Clinical Trials

Role of Patient-controlled Epidural Analgesia After Total Hip Replacement

Start date: September 1, 2014
Phase: N/A
Study type: Interventional

Total hip replacement (THR) is frequently followed by high pain experience. Epidural analgesia is a mainstay in postoperative treatment in patients after THR. The investigators found that patient-controlled epidural analgesia (PCEA) decreases total analgesics consumption compared to conventional method of analgesia based on physician's prescription while maintaining similar pain relief and safety profile. Therefore, PCEA should be considered the first choice method of analgesia in patients undergoing THR.