Diastolic Dysfunction PPCM in Patients With Documented Left Ventricular Systolic Function Recovery
Withdrawn
- Conditions
- Diastolic DysfunctionPeripartum Cardiomyopathy
- Interventions
- Diagnostic Test: A clinical Transthoracic echocardiogram
- Registration Number
- NCT04143997
- Lead Sponsor
- Medical College of Wisconsin
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
- Female.
- 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.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description PPCM with Diastolic Dysfunction & Normal Systolic Function A clinical Transthoracic echocardiogram The patient population examined will include patients diagnosed with peripartum cardiomyopathy who have diastolic dysfunction and normal systolic function.
- Primary Outcome Measures
Name Time Method Report the incidence of diastolic dysfunction in peripartum cardiomyopathy patients with full systolic function recovery 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Medical College of Wisconsin
🇺🇸Milwaukee, Wisconsin, United States