Exploring heart health in postmenopausal women
Official title: PGC-1, Purines and the Postmenopausal Heart
Run by Beth Israel Deaconess Medical Center · NCT06015776 · Data updated 2026-11-12
This study looks at how changes in estrogen levels may affect heart health in postmenopausal women and could lead to heart failure.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 30 Years to 88 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Beth Israel Deaconess Medical Center Academic / other |
| Locations | 1 site (Boston, Massachusetts) |
| Status | Recruiting |
| Started | July 1, 2019 |
| Main results expected | June 2030 |
| Study ends | June 2030 |
| Registry record updated | March 20, 2026 |
| Trial ID | NCT06015776 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are postmenopausal women undergoing cardiac surgery.
✕Probably not a fit
Patients with pre-existing heart conditions or those on hormone replacement therapy may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study investigates the role of purinergic signaling in diastolic heart failure among postmenopausal women. It focuses on how estrogen deficiency affects cardiac remodeling and mitochondrial metabolism, potentially leading to heart failure with preserved ejection fraction (HFpEF). Researchers will analyze cardiac tissue from patients undergoing cardiac surgery to understand the molecular pathways involved. The study aims to clarify the relationship between estrogen, purinergic signaling, and cardiovascular health in aging women.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of heart failure in postmenopausal women.
How similar studies have gone: Previous studies have indicated the importance of estrogen in cardiovascular health, suggesting potential for success in this area.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing cardiac surgery under cardiopulmonary bypass. Exclusion Criteria: * Refusal to participate * Emergency surgery * Pre-existing heart block * Preexisting atrial fibrillation * Redo surgery * Estrogen or hormone replacement therapy * History of chronic heart failure * History of major kidney disease
Where it's running
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Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States Recruiting
Study contacts
- Principal investigator: Robina Matyal, MD — Beth Israel Deaconess Medical Center, Professor of Anesthesia
- Study coordinator: Robina Matyal, MD
- Email: rmatyal1@bidmc.harvard.edu
- Phone: 6176401208
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Evaluating Cardiac Contractility Modulation in Heart Failure Patients
This study is testing a new heart treatment called Cardiac Contractility Modulation to see if it can help people with heart failure feel better and improve their heart function.
-
Remote rehabilitation for HFpEF patients using telerehabilitation
A home-based telerehabilitation program is being tested to see if it is safe and helpful for people with heart failure with preserved ejection fraction.
-
EDG-15400 in adults with HFpEF: a phase 2 study
This phase 2 study tests different doses of EDG-15400 against placebo in adults with HFpEF to see if it is safe and tolerable.
-
Incretin therapy with tirzepatide for obesity-related HFpEF
A 15-month study will test whether tirzepatide helps people with obesity and HFpEF by reducing plasma volume.
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Boosted exercise with group coaching for HFpEF
This trial tests a blended, guided exercise program with group coaching and remote monitoring to see if it helps older adults with HFpEF improve activity and health at a lower cost.
-
Exercise cardiac MRI for heart failure with preserved ejection fraction
This study will try low-field exercise cardiac MRI to see if it can diagnose, describe, and predict risk in people with HFpEF compared with those who have non-cardiac breathlessness and healthy volunteers.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.