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.
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