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Observational Registry on Patients With Endogenous CS to Document Safety and Effectiveness of Ketoconazole. — KetoPASS  

Cushing Syndrome Clinical Trial

Official title:
Prospective, Multi-country, Observational Registry to Collect Clinical Information on Patients With Endogenous Cushing's Syndrome to Assess Drug Utilization Pattern and to Document the Safety and Effectiveness of Ketoconazole.

Clinical Trial Summary

This is a non-interventional, prospective, multinational, multicentre, observational study, in which data collected are those derived from routine clinical practice via an European registry on CS: ERCUSYN.

Clinical Trial Description

The aim is to further document the safety and efficacy of Ketoconazole HRA administered in routine clinical practice in patients with CS. The study operates under real clinical practice conditions, i.e. there is no treatment protocol thus. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04872920
Study type Observational
Source HRA Pharma
Contact
Status Recruiting
Phase
Start date December 20, 2018
Completion date March 1, 2024
View Details
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