Use of Phenylephrine for Assessment of Mitral Regurgitation Severity

Recruiting Phase 1 Phase 2 Interventional Study
Mitral Regurgitation
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Diagnostic
Participants needed
35 (estimated)
Sponsor
Montefiore Medical Center · Other
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About This Trial
The study proposes to develop a phenylephrine protocol to be used during transesophageal echocardiography, whereby intravenous phenylephrine would be used to increase afterload with the intent to mimic the awake hemodynamic profile and variation that occurs with normal physical activity. The expectation is to see changes in severity of Mitral Regurgitation (MR) grade with increasing afterload, whi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients 18 years or older with MR on baseline echocardiographic evaluation who are scheduled to undergo TEE for further evaluation of mitral regurgitation. Exclusion Criteria: * The following patients will be excluded from the study: 1. Patients who are not clinically el…
Contacts

Mario Garcia, MD

718-920-4172

mariogar@montefiore.org

CONTACT

Waqas Hanif, MD

646-270-1421

whanif@montefiore.org

CONTACT