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NCT02785744

Genzyme Osteopenia/Osteoporosis Study

Completed Last updated 23 March 2021
What this trial tests

trial testing Gaucher disease DNA mutation analysis in Gaucher Disease in 76 participants. Completed in 1 September 2019.

Timeline
1 April 2016
Primary endpoint
1 September 2019
1 September 2019

Quick facts

Lead sponsorNYU Langone Health
StatusCompleted
Study typeOBSERVATIONAL
Enrollment76
Start date1 April 2016
Primary completion1 September 2019
Estimated completion1 September 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

NYU Langone Health — full company profile →

Who can join

18 and older, any sex, with Gaucher Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Gaucher disease is a most common genetic metabolic disease characterized by low platelet number, liver and spleen enlargement and various forms of bone diseases including low bone mineral density leading to brittle bones. Various treatment options are now available for this disease. The purpose of this research study is to determine the prevalence of Gaucher disease in patients with low bone mineral density as observed by DEXA scan, which is a form of X-Ray of the bone.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Gaucher Disease

Currently open trials in the same condition.

Other NYU Langone Health trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02785744.

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