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Latest
Clinical Trials in the EU / 2024-520086-31-00
Authorised, recruiting Phase IV

HYDrochlorothiazidE compared to valsartan to treat arterial hypertension in patients with Hypertrophic obstructive CardioMyopathy – the multicenter, randomized, double-blind, controlled, crossover HYDE-HCM Trial

2024-520086-31-00 · tracked via the Priya Life Science EU tracker
Sponsor type
Educational Institution
Therapeutic area
Cardiovascular Diseases
Decision date
29/12/2025
Enrollment target
40
Sites
Austria

Condition studied

Hypertrophic cardiomyopathy

Investigational medicinal product(s)

HCT G.L. 50 mg-TablettenValsartan Sandoz 160 mg - Filmtabletten

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Difference in absolute change of peak LVOT gradient at rest from before to after the treatment period between the two interventions

Endpoint detail

Difference of absolute changes between the two intervention groups of Peak LVOT gradient after Valsalva-Maneuver, Difference of absolute changes between the two intervention groups of left ventricular systolic pressure calculated from brachial blood pressure and LVOT gradient, Difference of absolute changes between the two intervention groups of Kansas City Cardiomyopathy Questionnaire (KCCQ-23 Score), Difference of absolute changes between the two intervention groups of EQ5D5L score, Difference of absolute changes between the two intervention groups of NT-proBNP, Difference of absolute changes between the two intervention groups of High-sensitive Troponin T/I, Difference of absolute changes between the two intervention groups of Interleukin-6, Difference of absolute changes between the two intervention groups of pVO2 during CPET (CPET sub-study), Difference of absolute changes between the two intervention groups of mean systolic postprandial office blood pressure, Difference of absolute changes between the two intervention groups of mean diastolic postprandial office blood pressure, Number of serious adverse events (SAEs), Difference of absolute changes between the two intervention groups of NYHA class

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2024-520086-31-00 on CTIS ↗ ← All trials in the EU