Rotator Cuff Arthropathy

4

Review clinical trials related to Rotator Cuff Arthropathy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Prosthesis Versus Active Exercise Program in Patients With Rotator Cuff Arthropathy

Reverse shoulder arthroplasty (RSA) is a well-established treatment for rotator cuff arthropathy. However, the effectiveness of RSA has not been compared to non-surgical treatment in a randomised controlled trial. Shoulder exercises may be an effective treatment for reducing pain and improving function in glenohumeral osteoarthritis. The primary aim of this trial is to examine if RSA followed by standard postsurgical rehabilitation is superior to a 12-week exercise programme in patients with rotator cuff arthropathy eligible for unilateral RSA. The investigators hypothesise that surgical intervention followed by standard rehabilitation, results in clinically relevant (14-point, on a scale from 0-100) improvement compared to the exercise intervention.

Participants needed: 102
Trial details
Age: 60-85Biological sex: AllType: InterventionalSponsor: University of AarhusUpdated: Jul 2, 2026Locations: 8
Eligibility criteria

Patients 60-85 years [+2]

Previous shoulder fracture (fracture of the proximal humerus or glenoid fracture... [+6]

Status: Recruiting

Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Shoulder Prosthesis System

This study is designed as a prospective, multicenter, observational post-market clinical follow-up (PMCF) study to evaluate the safety and effectiveness of the Tipmed™ Shoulder Prosthesis System at 12 months postoperatively. The study population includes adult patients who undergo reverse shoulder arthroplasty (RSA) or shoulder hemiarthroplasty (HA) using the Tipmed™ implant systems due to various clinical indications such as osteoarthritis, rotator cuff arthropathy, or proximal humerus fractures. The main objective is to gather real-world clinical evidence on the 12-month post-operative safety profile, potential complications, and functional outcomes of the device during routine clinical practice.

Participants needed: 54
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: TIPMED Medical Device Manufacturing Ltd. Co.Updated: Jul 1, 2026Locations: 4
Eligibility criteria

Individuals aged 18 years and older, [+5]

Concurrent participation in any other interventional clinical trial.

Status: Recruiting

RETRO-PROSPECTIVE POSTMARKET CLINICAL STUDY FOR FX SHOULDER SOLUTIONS SHOULDER SYSTEMS

This study takes place in the framework of the PostMarket Clinical Follow-up plan of the Shoulder Systems commercialized by FX SHOULDER SOLUTIONS. The included cases will be followed for 10 years after index surgery. Primary objective is the assessment in real life of the revision rate of the shoulder systems at long-term. Secondary objectives are * Revision rate at each post op visit * Range of motion at each post op visit * Quick Dash, Constant, American Shoulder and Elbow Surgeons Shoulder Score (ASES), Subjective Shoulder Value (SSV), Pain scores at each post op visit * Radiological assessment of implant positioning through geometrical parameters at each post op visit * Incidence of complications at each post op visit * Qualitative feedback from surgeons on the instrumentation

Participants needed: 1,004
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: FX SolutionsUpdated: Apr 30, 2026Locations: 22
Eligibility criteria

Indication for hemi or total shoulder replacement with one of the FX SHOULDER SO... [+3]

Neurological pathologies compromising the shoulder stability [+2]

Status: Recruiting

Corticosteroid Injection Versus Nerve Block

The purpose of this study is to evaluate conservative pain relief measures for patients suffering from glenohumeral arthritis or rotator cuff arthropathy. Conservative management of osteoarthritis is often first line treatment, and while a corticosteroid injection is frequently used, suprascapular nerve blocks have not often been described as an analgesic option in this population.

Participants needed: 40
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University of MinnesotaUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

diagnosis of glenohumeral osteoarthritis, rheumatoid arthritis, or rotator cuff...

uncontrolled diabetes (patients will be excluded if no HbA1c within a year or if... [+6]