Marfan Syndrome Clinical Trial
Official title:
Effects of Atenolol, Perindopril and Verapamil on Haemodynamic and Vascular Function in Marfan Syndrome - A Randomised Double-Blind Crossover Trial
The investigators are looking at the different impacts of atenolol, verapamil and perindopril on large artery and lv function in marfan syndrome. It is a double-blind, randomised cross-over trial.
The investigators recruited 21 patients with confirmed diagnosis of Marfan syndrome from two
centres. The investigators performed radial artery applanation tonometry and pulse wave
analysis to derive central aortic pressure and haemodynamic indexes pre-and post
administering Atenolol 75mg, Perindopril 4mg and Verapamil 240mgs each for four weeks with a
two week wash-out between medications. All patients underwent detailed functional and
anatomical echocardiographic assessments at each visit.
Inclusion criteria were ages 16-60 years with no treatment or β-blocker or other monotherapy
only for Marfan syndrome. Patients with previous aortic dissection or aortic surgery, severe
valvular regurgitation, aortic diameter at the sinotubular junction ≥ 5.0cm,
contraindications to specific drug treatment, e.g. asthma and β-blocker, or those who were
pregnant or at risk of pregnancy were excluded.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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