Last updated: March 24, 2021
Sponsor: Steen Hvitfeldt Poulsen
Overall Status: Completed
Phase
2
Condition
Heart Defect
Heart Disease
Cardiomyopathy
Treatment
N/AClinical Study ID
NCT03532802
1-10-72-441-17
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Wall thickness ≥ 15 mm in one or more myocardial segments that is not explained byloading conditions.
- LVOT gradient > 30 mmHg at rest and/or > 50 mmHg at Valsalva's maneuver or exercise
- New York Heart Association Functional class (NYHA) ≥ II
Exclusion
Exclusion Criteria:
- Age < 18 years
- Known allergy to trial medicine
- Contraindications to beta-blocker treatment
- Contraindications to Magnetic resonans scan, including contraindication to thecontrast agent gadolinium.
- Female patients who are pregnant (positive plasma-HCG), breastfeeding or ofchild-bearing potential while not practicing effective chemical contraceptivehormones.
- In case of patients having a pacemaker, they may not be pace-dependent.
- Treatment with Amiodarone
- Atrial fibrillation/flutter at the time of examination
- Bradycardia < 49 beats/min
- Systolic blood pressure < 100 mmHg
- Trifascicular block
- Previous transcoronary ablation of septum hypertrophy (TASH) or myectomy
- Current abuse of alcohol and/or drugs
- Significant co-morbidity or issues that makes the patient unsuitable forparticipation, judged by the investigator
- Patients who cannot give valid consent (e.g. mental illness or dementia)
- Patients who do not understand danish
Study Design
Total Participants: 30
Study Start date:
May 01, 2018
Estimated Completion Date:
September 01, 2020
Study Description
Connect with a study center
Aarhus University Hospital, Department of Cardiology
Aarhus N, Danmark 8200
DenmarkSite Not Available

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