Diastolic Dysfunction PPCM in Patients With Documented Left Ventricular Systolic Function Recovery

Medical College of Wisconsin1 site in 1 countryNovember 1, 2019

ConditionsPeripartum Cardiomyopathy Diastolic Dysfunction

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Peripartum Cardiomyopathy
Sponsor: Medical College of Wisconsin
Locations: 1
Primary Endpoint: Report the incidence of diastolic dysfunction in peripartum cardiomyopathy patients with full systolic function recovery
Status: Withdrawn
Last Updated: last year

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this project is to evaluate parameters of diastolic dysfunction assessed by clinical echocardiogram in patients who have had recovery of systolic function.

Registry

clinicaltrials.gov

Start Date

November 1, 2019

End Date

January 29, 2021

Last Updated

last year

Study Type

Observational

Sex

Female

Investigators

Sponsor

Medical College of Wisconsin

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Greater than age 18 years at the time of peripartum cardiomyopathy diagnosis.
•Adults with a current or prior diagnosis of peripartum cardiomyopathy and documented recovered of left ventricular systolic function.
•Documented recovered of LV systolic performance defined as LVEF \> 50%.

Exclusion Criteria

•No pregnancy history.
•No diagnosis of peripartum cardiomyopathy.
•Non-recovery of LV systolic function.

Outcomes

Primary Outcomes

Report the incidence of diastolic dysfunction in peripartum cardiomyopathy patients with full systolic function recovery

Time Frame: January 1, 2014 through September 1, 2019

Investigators will review and report incidence of remaining diastolic dysfunction for local patient population which have recovered systolic function.