NCT03409718Active, not recruiting
Database Retrieval for the Comprehensive Shoulder
Comprehensive Shoulder System Database Retrieval
Source: ClinicalTrials.gov · Last updated 10 Jul 2026
Brief summary (registry, in English)
This study is a retrieval of database information regarding survivorship of the Comprehensive Shoulder System family of products. The primary objective of the retrieval is to collect data that will contribute to the post market surveillance requirements for this product and will provide feedback to design engineers, support marketing efforts and publications, and answer potential questions form reimbursement agencies.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 160 (actual)
- First submitted
- 18 Jan 2018
- Start date
- 24 Feb 2011
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Zimmer Biomet
- Diseases
- Rheumatoid arthritis
- NCT number
- NCT03409718
What you commit to
- Study type: Observational
- Participants enrolled: 160
- From 24 Feb 2011 to the primary completion date, 31 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Absolute contraindications include infection, sepsis, and osteomyelitis.
- Uncooperative patient or patient with neurologic disorders who is incapable or unwilling to follow directions.
- Metabolic disorders which may impair bone formation.
- Distant foci of infections which may spread to the implant site.
Other
- Osteoporosis.
- Osteomalacia.
- Rapid joint destruction, marked bone loss or bone resorption apparent on roentgenogram.
Who the study is looking for
- Must have one of the following indications:
- Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis.
- Rheumatoid arthritis
- Revision where other devices or treatments have failed.
- Correction of functional deformity.
- Fractures of the proximal humerus, where other methods of treatment are deemed inadequate.
- Difficult clinical management problems, including cuff arthropathy, where other methods of treatment may not be suitable or may be inadequate.
- Need to obtain pain relief and improve function
- Ability and willingness of the patient to follow instructions, including control of weight and activity level
- A good nutritional state of the patient
- The patient must have reached full skeletal maturity
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Acromion LLC Coordinator of this site? Confirm its status | Towson | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.