πŸ›οΈ Verified NIH Record β€’ Updated 2025-07-16

Use of Phenylephrine for Assessment of Mitral Regurgitation Severity (NCT04500899)

Evaluating the Severity of Mitral Regurgitation Using Phenylephrine During Transesophageal Echocardiography

🟒 Recruiting Phase1 / Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Montefiore Medical Center

🩺 Plain-English Summary (8th-Grade Level)

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, which in turn can provide more accurate quantification of MR severity to assist in clinical decision making.

Who can join: Review the eligibility criteria below.

Location: Montefiore Medical Center β€” New York, New York

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • Montefiore Medical Center β€” New York, New York

πŸ“ž Contact the Study Coordinator

Phone: (718) 920-4172

Email: mariogar@montefiore.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—