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

Withdrawn
Conditions
Diastolic Dysfunction
Peripartum 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WITHDRAWN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
  1. Female.
  2. Greater than age 18 years at the time of peripartum cardiomyopathy diagnosis.
  3. Adults with a current or prior diagnosis of peripartum cardiomyopathy and documented recovered of left ventricular systolic function.
  4. Documented recovered of LV systolic performance defined as LVEF > 50%.
Exclusion Criteria
  1. No pregnancy history.
  2. No diagnosis of peripartum cardiomyopathy.
  3. Non-recovery of LV systolic function.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
PPCM with Diastolic Dysfunction & Normal Systolic FunctionA clinical Transthoracic echocardiogramThe patient population examined will include patients diagnosed with peripartum cardiomyopathy who have diastolic dysfunction and normal systolic function.
Primary Outcome Measures
NameTimeMethod
Report the incidence of diastolic dysfunction in peripartum cardiomyopathy patients with full systolic function recoveryJanuary 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
NameTimeMethod

Trial Locations

Locations (1)

Medical College of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

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