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Joint Diseases clinical trials

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NCT ID: NCT03773640 Completed - Clinical trials for Temporomandibular Joint Dysfunction Syndrome

The Application of Radio Frequency Waves

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

The aim of the study was to evaluate the influence of radio waves on the functioning of masseter muscles in the course of painful functional disorders of the organ, and thus the usefulness of these procedures in the treatment supporting temporomandibular joint dysfunction. Material and method The study group I (20 patients) and control group II (20 patients) consisted of patients, aged 19 to 45 years, of both sexes, who reported to the Consulting Room of Temporomandibular Joint Dysfunction in Institute of Dentistry in Krakow to undertake prosthetic treatment of pain form of temporomandibular disorders with the dominant muscle component. Study group (I) consist of patients who were treated with the occlusal splints and radio frequency currents. In the case of application of radiation to the muscle area, the energy was 20 J and 15 J to the area of the masticatory muscles, the frequency was 3 MHz, bipolar technique, the duration of the procedure was 10 minutes, the coupling substance was a gel for ultrasound examinations. The control group ( II) consisted of 20 patients treated with occlusion splints and sonophoresis procedures. For the area of mastication muscles 0.9 W/cm² treatments were applied, the duty factor was 80%, the treatment time was 10 minutes, and the medical substance was 25%Voltaren gel.

NCT ID: NCT03771430 Recruiting - Clinical trials for Degenerative Joint Disease of Knee

A Multidisciplinary Intervention in Total Knee Arthroplasty

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

The purpose of this study is to investigate the effectiveness of cognitive behavioral therapy delivered as an e-therapy program, combined with physical exercise delivered by physiotherapists, for patients on waiting list for total knee arthroplasty. The patients will be randomized to either 1) a non-surgical program consisting of web-based cognitive behavioral therapy combined with physiotherapy, 2) total knee arthroplasty (TKA) surgery followed by web-based cognitive behavioral therapy combined with physiotherapy, or 3) a control group who undergo TKA followed by standard physiotherapy.

NCT ID: NCT03768128 Active, not recruiting - Clinical trials for Non-inflammatory Degenerative Joint Disease (NIDJD) of the Knee

Safety and Performance of the Journey™ II UNI Unicompartmental Knee System

JII-Uni
Start date: August 10, 2018
Phase:
Study type: Observational

This clinical study will evaluate the early to midterm safety and performance of the JOURNEY™ II UNI UKS in patients with non-inflammatory degenerative joint disease of the knee requiring lateral or medial knee compartment replacement. Clinical, radiographic, health economic and safety outcomes will be evaluated.

NCT ID: NCT03766464 Completed - Clinical trials for Temporomandibular Joint Disorders

Aspects Associated With Obstructive Sleep Apnea, Bruxism and Orofacial Pain

Start date: January 1, 2019
Phase:
Study type: Observational

This study evaluated the influence of the sleep bruxism (SB), awake bruxism (AB) and obstructive sleep apnea syndrome (OSAS) on the signs and symptoms of temporomandibular disorders (TMD).

NCT ID: NCT03765723 Not yet recruiting - Anesthesia Clinical Trials

Prediction Model of Acute Postoperative Pain in Bilateral Total Knee Replacement Arthroplasty Patient

Start date: January 1, 2019
Phase:
Study type: Observational

This study aims to predict risk factors of acute postoperative pain of the patients undergoing Total Knee Replacement Arthroplasty(TKRA).

NCT ID: NCT03740412 Completed - Osteoarthritis Clinical Trials

Study to Reduce Sitting in Older Adults Undergoing Hip or Knee Replacements

INTEREST
Start date: January 29, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the feasibility of an intervention to reduce sedentary behaviour in older adults waiting for hip and knee replacements. The study will be a randomised controlled trial design, including 2:1 randomisation into an intervention and usual care group respectively. A target of n=45 patients ≥60 years will be recruited from Russells Hall Hospital, Dudley, UK, approximately 8-10 weeks before surgery, assisted by research nurses. The variable-length intervention, informed by Self-Determination Theory (SDT), will be composed of multiple behaviour change techniques, namely motivational interviewing, individualised feedback on sedentariness, goal-setting, environmental modification, self-monitoring, and social support. Assessments will occur at baseline, 1 week pre-surgery, and 6 weeks post-surgery. The primary outcome will be the feasibility of the trial, assessed quantitatively using study statistics, and with mixed-methods assessment of acceptability, practicality, adaption, satisfaction, and safety via questionnaires given to participants. Exploratory outcomes will include physical function, cardiometabolic biomarkers, measurement of SDT constructs, and both objective and subjective measurement daily activity and sedentariness. The study will last up to 18 weeks per participant.

NCT ID: NCT03736408 Completed - Clinical trials for Temporomandibular Disorders

Frequency of Occurrence of the Pain Form of Temporomandibular Joint Dysfunction

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

Temporomandibular joint dysfunction (TMJD) includes disorders of the masticatory muscles in the stomatognathic system, temporomandibular joints and the surrounding structures. They are often associated with abnormal conditions of occlusion. The term "functional disorders" does not include all diseases of the muscular and joint system, like inflammatory, degenerative changes and cancer lesions of the muscles (multiple sclerosis, tetany, dermatomyositis). They are often the result of excessive and prolonged muscle hyperactivities and excessive work that cause non-physiological loads occurring in temporomandibular joints

NCT ID: NCT03735173 Completed - Shoulder Pain Clinical Trials

Comparing the Outcome of Cemented All-Polyethylene Pegged vs. Keeled Components Through a Subscapularis Tenotomy or a Subscapularis Peel

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

Participants who choose to participate in this study, will either have their tendon repaired to tendon, so-called tenotomy repair, or tendon repaired to bone, so-called peel repair.

NCT ID: NCT03727490 Active, not recruiting - Clinical trials for Arthropathy Shoulder

The Role of Subscapularis Repair in Reverse Shoulder Arthroplasty

Start date: January 2017
Phase: N/A
Study type: Interventional

The overall goal of the study is to determine if repairing the subscapularis tendon during primary reverse shoulder arthroplasty effects short-term patient outcomes. The study is a patient blinded randomized controlled trial that is currently enrolling.

NCT ID: NCT03726788 Not yet recruiting - Clinical trials for Magnetic Resonance Imaging

Intra Articular Injection of Botulinum Toxin Versus Corticoids in Gonarthrosis

TOXART
Start date: September 2019
Phase: Phase 2
Study type: Interventional

We believe we can demonstrate a link between the analgesic action of intra-articular injection of botulinum toxin and synovial inflammation by Dynamic Contrast Enhancement (DCE) perfusion Magnetic Resonance Imaging (MRI).