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Joint Diseases clinical trials

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NCT ID: NCT02589197 Completed - Joint Disease Clinical Trials

Gait and Functional Outcomes Study Following Total Knee Arthroplasty With Medial-pivot or Posterior-stabilized Implants

GOLD
Start date: July 13, 2016
Phase:
Study type: Observational

MicroPort Orthopedics (MPO) is conducting this study to build upon the results of a previous study which showed the Medial Pivot (MP) system required lower quadriceps activation than subjects implanted with a Posterior stabilized (PS) system preforming the same activities of daily living.

NCT ID: NCT02584725 Completed - Arthropathy of Knee Clinical Trials

Tranexamic Acid Dosing for Total Joint Arthroplasty

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of increasing doses of tranexamic acid (TXA) on limiting blood loss during total knee and total hip arthroplasty as defined by a change in hemoglobin from pre-operative baseline to the first post-operative day.

NCT ID: NCT02554474 Completed - Clinical trials for Rheumatoid Arthritis

OPAM-IA: Using Digital Activity Trackers to Improve Physical Activity in Inflammatory Arthritis

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

Being physically active can reduce pain and fatigue, improve mobility and enhance quality of life in people with arthritis, but adherence to an active lifestyle is poor, with less than half of people with arthritis being active. The primary goal of this randomized controlled trial is to assess the efficacy of a physical activity coaching model to improve physical activity participation and reduce sedentary time in patients with Rheumatoid Arthritis and Systemic Lupus Erythematosus. This model combines the use of a Fitbit Flex (wireless physical activity tracker) paired with a FitViz application, a group education session, and telephone counselling by a physiotherapist.

NCT ID: NCT02543463 Completed - Clinical trials for Degenerative Joint Disease

Navigation With X3 vs Non-Navigation With X3 Study

Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of the large head in THA with a navigation system and without a navigation system.

NCT ID: NCT02542592 Completed - Osteoarthrosis Clinical Trials

Effect of Methylprednisolone on Immune Signaling in Hip-arthroplasty Patients

Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The study evaluates the pathophysiological effects of a single dose Methylprednisolone administered prior to total hip-arthroplasty (THA) surgery. The investigators examine the effect on immune signaling and recovery after surgery. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving Methylprednisolone will experience a positive modulation of the immune response and an enhanced recovery.

NCT ID: NCT02540863 Completed - Clinical trials for Temporomandibular Joint Disorders

Miofascial Release and Exercises Therapy in the Treatment of Temporomandibular Disorders

Start date: June 2015
Phase: N/A
Study type: Interventional

Objectives: The aim of this research is to compare the effectiveness of myofascial release therapy and exercise therapy on pain, quality of sleep, anxiety, trigger points, and joint sounds in individuals with temporomandibular disorders and myofascial pain-dysfunction syndrome. Material and Methods: A single-blind randomized clinical trial will be conducted in a university research clinic. Sixty-four subjects with temporomandibular disorders and myofascial pain-dysfunction syndrome will be randomly assigned to physical therapy group (myofascial release protocol and Rocabado exercise therapy) and control group (exercise therapy). Intensity of pain, quality of life, quality of sleep, anxiety, trigger points, and joint sounds will be collected at baseline, and forty-eight hours after the intervention phase.

NCT ID: NCT02512536 Completed - Clinical trials for Rotator Cuff Tear Arthropathy

Does Botulinum A Toxin Help With Pain From Rotator Cuff Arthropathy?

Start date: July 2016
Phase: Phase 2
Study type: Interventional

Rotator cuff arthropathy is a cause of shoulder arthritis which is a common condition seen both in primary and secondary care. It is a painful condition, with significant disability. Specialist shoulder replacements have found acceptance within the trust, nationally and internationally although there are high complication rates. There is however a significant cost difference (fifty fold) between a reverse total shoulder replacement and a botox injection, and to date there have been no randomised control trials, or any registered, comparing the use of a botox injection for pain relief in cuff arthropathy versus no treatment. If there is a significant clinical difference in the pain outcomes between the two, this could result in significant savings to the NHS and the taxpayer as a whole. If high levels of pain relief could be predictably obtained using Botulinum A toxin injections then potentially patients could avoid the need for surgery.

NCT ID: NCT02510924 Completed - Nasal Obstruction Clinical Trials

Role of Airtraq Mobile to Improve Intubation Conditions With Airtraq

AirtraqMob
Start date: August 2015
Phase: N/A
Study type: Interventional

Airtraq sp has been proven effective for intubating patients presenting with difficult airway. The Airtraq sp allows visualisation of the tracheal inlet only for the intubator. By adding a smartphone with a dedicated app (Airtraq Mobile) to the Airtraq sp, the visualisation of the tracheal inlet is possible for all the airway providers. The investigators aim to demonstrate that the addition of the Airtraq Mobile app improves success rate of intubation (primary endpoint), as well as confort of the airway provider, shortens time for intubation and reduces injury to the patients.

NCT ID: NCT02508428 Completed - Osteoarthritis Clinical Trials

Marathon and Enduron Polyethylene at Long-Term Follow-up

Start date: January 6, 1999
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether crosslinked Marathon and standard Enduron polyethylene liners show differences in survivorship due to wear-related revisions at minimum 14-year follow-up and every 5 years after.

NCT ID: NCT02493621 Completed - Arthropathy of Hip Clinical Trials

Compare Epidural vs. Lumbar Plexus Analgesia After Hip Arthroplasty

Start date: December 2014
Phase:
Study type: Observational

The goal of this retrospective chart review is to evaluate if the implementation of lumbar plexus block placement for postoperative pain have improved conditions in the postoperative period for patients undergoing total hip arthroplasty when compared to the placement of epidurals for postoperative pain management.