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Rotator Cuff Tear Arthropathy clinical trials

View clinical trials related to Rotator Cuff Tear Arthropathy.

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NCT ID: NCT06316050 Completed - Rotator Cuff Tears Clinical Trials

Retrovertion Assesment and Study in Elderly Patients With Reverse Total Shoulder Arthroplasty

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

Determine the optimal degree of retroversion (0-30º) to obtain the best rotational mobility, both internal and external, of the shoulder after implanting a reversed sghoulder arthroplasty (Comprehensive system), and analyze the functional and radiologic results based on humeral retroversion.

NCT ID: NCT04415931 Completed - Clinical trials for Shoulder Osteoarthritis

Local Infiltration Analgesia Vs. Interscalene Block in Total Shoulder Arthorplasty

Start date: August 15, 2020
Phase: N/A
Study type: Interventional

Pain management following total shoulder arthroplasty is an important factor in determining patient outcomes and satisfaction. Interscalene brachial plexus blockade has been used successfully to minimize pain in the acute post-operative period. While shown to be effective, interscalene blockade has known complications. In addition, interscalene block has been shown to be significantly more expensive when compared to local anesthesia infiltration. Local anesthetics such as bupivacaine have long been used to assist in post-operative anesthesia. Recent reports have demonstrated local infiltration of liposomal bupivacaine to be similar to interscalene block in regards to patient analgesia even in the first 24 hours post operatively, with the added benefit of lower complications and costs. While most reports examine the efficacy of local infiltration with liposomal bupivacaine in the shoulder, other total joint literature has been positive regarding the use of local infiltration analgesic mixture for improved post-operative analgesia using a multi-modal approach to infiltrative analgesia. Despite these reports, the role and efficacy of local infiltration analgesia in shoulder arthroplasty is lacking. The purpose of the proposed study is to determine the efficacy and safety of local infiltration analgesia in shoulder arthroplasty in comparison to interscalene block through a randomized prospective clinical trial. Our hypothesis is that local infiltration analgesia will lead to postoperative pain scores, opiate consumption, and complication rate that are not significantly different from interscalene block.

NCT ID: NCT03111147 Completed - Clinical trials for Rotator Cuff Tear Arthropathy

Impact of Humeral Component Version on Outcomes Following RTSA

Start date: May 12, 2017
Phase: N/A
Study type: Interventional

The proposed study is a prospective, single-blinded, randomized trial to investigate the impact of humeral component version on shoulder range of motion and patient reported functional outcomes following reverse total shoulder arthroplasty.

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: NCT02466321 Completed - Clinical trials for Cuff-tear Arthropathy

Anatomical Shoulderâ„¢ Inverse/Reverse Study

Start date: September 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to obtain outcomes data on the Anatomical Shoulderâ„¢ Inverse/Reverse System by analysis of standard scoring systems and radiographs. Outcome data will be collected using the following standard scoring systems of which summary statistics will be provided: - Constant and Murley Score to evaluate clinical parameters such as range of motion, power, level of pain and functional ability. - SF-12 Physical and Mental Health Summary Measures (SF12 Questionnaire) comprising of twelve questions to assess the subject's physical and mental health status which must be answered by the patient.

NCT ID: NCT02084693 Completed - Osteoporosis Clinical Trials

COMPREHENSIVE® REVERSE SHOULDER Mini BasePlate

Start date: December 2013
Phase:
Study type: Observational

Evaluate Survivorship for the Biomet® Comprehensive® Reverse Shoulder Mini Baseplate.

NCT ID: NCT02052466 Completed - Osteoarthritis Clinical Trials

Prediction of Development of Scapular Notching Following Reverse Total Shoulder Arthroplasty

Start date: January 2014
Phase: N/A
Study type: Observational

The hypothesis is that computer simulated bony impingement of the bone surrounding the spherical glenoid implant (the glenosphere) along the scapular neck on three-dimensional (3-D) computed tomography (CT) imaging analysis is predictive of the location of clinical scapular notching that develops following reverse total shoulder arthroplasty (TSA).

NCT ID: NCT01954433 Completed - Rotator Cuff Tear Clinical Trials

Costs and Consequences of Three Common Orthopedic Procedures on the Upper Extremity

Start date: November 2013
Phase:
Study type: Observational

This study compares costs and effectiveness / utility of three common orthopedic surgeries in shoulder and hand from the perspective of the Swiss health system and the clinic. The cost of health care is continuously rising, making economic considerations part of the decision process, in particular for the allocation of available resources. However, cost-effectiveness and cost-utility studies of interventions in the upper extremities are rare. The purpose of this study is to gain more information and to provide a basis for the decision process.

NCT ID: NCT01778777 Completed - Clinical trials for Rotator Cuff Tear Arthropathy

Safety Study of Univers® Revers Shoulder Prosthesis

Start date: September 1, 2013
Phase: N/A
Study type: Interventional

The primary safety objective is to demonstrate that severe device-related complication (Serious Adverse Device Effect = SADE) occur within 2 years after prosthesis implantation at a rate of less than 2%. Such adverse events include (but are not limited to) revisions due to dislocation or glenoid loosening, septic arthritis and scapular fractures requiring surgical repair.

NCT ID: NCT01687894 Completed - Clinical trials for Rotator Cuff Tear Arthropathy

Vasopressin to Prevent Hypotension During Beach Chair Surgery

Start date: May 2012
Phase: N/A
Study type: Observational

Patients undergoing surgery in beach chair position (BCP) are at risk for cerebral ischaemia. The impacts of arginine vasopressin (AVP) on haemodynamics and cerebral oxygenation are evaluated during surgery in BCP.