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Chondrocalcinosis clinical trials

View clinical trials related to Chondrocalcinosis.

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NCT ID: NCT04176003 Completed - Clinical trials for CPPD - Calcium Pyrophosphate Deposition Disease

Perspectives on CPPD Outcome Domains

Start date: October 8, 2019
Phase:
Study type: Observational

The purpose of this study is to obtain patient and stakeholder perspectives on what outcome measures should be included in future trials on CPPD (Calcium PyroPhosphate Deposition), a common form of inflammatory arthritis. This will form part of a wider OMERACT (Outcome Measures in Rheumatology) study, involving multiple international sites, to determine a core domain set (an agreed set of outcome measures) for this disease. In the UK, up to 10 patients with CPPD and their caregivers, healthcare professionals who care for patients with CPPD, and other stakeholders, which may include government organisations, non-government organisations, pharmaceutical representatives and health advocacy groups, will be invited to participate in a single, semi-structured interview. Interviews will be face-to-face or telephone, last up to one hour and digitally audio-recorded. For patients and their caregivers, interviews will explore their lived experience of CPPD, its impact on their daily lives, and the perceived relevance of outcome measures used in previous studies. For healthcare professionals and other stakeholders, interviews will explore their experience dealing with patients with CPPD, how they perceive CPPD impacts patient lives, and the perceived relevance of the outcome measures used in previous studies. Following analysis of the data, participants will be sent a short report with the researchers' findings, and asked to check the accuracy of these and provide brief written feedback. Interviews will also take place with patients, caregivers, healthcare practitioners and stakeholders at the other international sites where ethics committee approval will be sought locally. It is anticipated that around 30 participants will be recruited across all sites. Analysis of all interviews will be primarily conducted and managed at the UK site.

NCT ID: NCT03128905 Completed - Chondrocalcinosis Clinical Trials

Trial of Colchicine Versus Prednisone for the Treatment of Acute CPPD Arthritis

COLCHICORT
Start date: February 5, 2018
Phase: Phase 3
Study type: Interventional

Chondrocalcinosis, recently renamed the calcium pyrophosphate deposition (CPPD) disease, is a very frequent affection of the elderly and causes very painful arthritis. International recommendations for the treatment of patients suffering from CPPD are based upon rare studies, not randomized, with small samples, and thus very weak scientific evidence. The treatment of CPPD arthritis is extrapolated from the experience of gout treatment, another crystal deposition disease. Among recommended treatments, colchicine and oral steroids are recommended as first-line treatments, while NSAIDs are used with caution in elderly populations of patients. Colchicine utilization is not risk-free, in particular with old patients and patients with renal impairment. Drug interactions of colchicine can have serious consequences, especially in a polymedicated old patient's population. Oral steroids are an interesting alternative in this indication with a potential of being better tolerated, but comparative efficacy with colchicine needs to be studied. From a broader point of view, colchicine and oral steroids have never been compared in any crystal related arthritis. This is the first large randomized controlled trial for CPPD acute arthritis.

NCT ID: NCT02243631 Completed - Clinical trials for Calcium Pyrophosphate Deposition Disease

Effect of Probenecid on Synovial Fluid ATP Levels in CPPD

Start date: October 15, 2014
Phase: Early Phase 1
Study type: Interventional

This study will investigate the hypothesis that probenecid, a medication currently used for gout, reduces levels of ATP in the joint fluid of patients with calcium pyrophosphate deposition disease (CPPD), another common type of crystal-related arthritis. There is good evidence that CPPD results from an excess of ATP in joints. The investigators will measure levels of ATP in joint fluid before and after 5 days of treatment with probenecid. This study will serve to rationalize larger studies of probenecid in CPPD.

NCT ID: NCT01529099 Completed - Osteoarthritis Clinical Trials

Postmarketing Study to Determine Performance of the SIGMA HP® PARTIAL KNEE SYSTEM

Start date: January 2009
Phase: Phase 4
Study type: Interventional

This is a postmarketing study to assess the overall performance and survivorship of the SIGMA HP® PARTIAL KNEE SYSTEM.

NCT ID: NCT00797537 Completed - Chondrocalcinosis Clinical Trials

Ultrasound and X-ray in Detecting Articular Cartilage Calcification

chondro
Start date: May 2008
Phase: N/A
Study type: Interventional

Prospective study with an echography of the 2 knees and radiography of the 2 knees (front and profile) for each patient. If found calcification on ultrasound further examination with ultrasound wrists, hips and shoulders.

NCT ID: NCT00453128 Completed - Chondrocalcinosis Clinical Trials

Diagnostic Rentability of Screening for Associated Conditions in Calcium Pyrophosphate Deposition Disease Patients

Start date: January 1997
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether thorough analytical evaluation is useful to diagnose metabolic conditions associated to calcium pyrophosphate deposition disease.