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Non-interventional Study on Osilodrostat in Patients With Endogenous Cushing's Syndrome

NCT05382156

This is a non-interventional, multinational, multi-centre study with primary data collection, to further document the safety and efficacy of osilodrostat administered in routine clinical practice in patients treated with osilodrostat for endogenous Cushing's Syndrome

Endogenous Cushing's Syndrome

RECORDATI GROUP206 participantsStarted Jun 2022

Phoenix, Arizona, United States • Atlanta, Georgia, United States • Chicago, Illinois, United States +40 more locations

COMPLETED

Cardiovascular Status in Patients With Endogenous Cortisol Excess (Cushing's Syndrome)

NCT03880513

Within this trial, the cardiovascular and mental status as well as the metabolic profiles of patients with endogenous cortisol excess are evaluated.

Endogenous Cushing's Syndrome

Wuerzburg University Hospital108 participantsStarted Oct 2014

Würzburg, Bavaria, Germany

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Non-interventional Study on Osilodrostat in Patients With Endogenous Cushing's Syndrome

Cardiovascular Status in Patients With Endogenous Cortisol Excess (Cushing's Syndrome)

Non-interventional Study on Osilodrostat in Patients With Endogenous Cushing's Syndrome

Cardiovascular Status in Patients With Endogenous Cortisol Excess (Cushing's Syndrome)