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

Medical College of Wisconsin logo

Medical College of Wisconsin

Status

Withdrawn

Conditions

Peripartum Cardiomyopathy
Diastolic Dysfunction

Treatments

Diagnostic Test: A clinical Transthoracic echocardiogram

Study type

Observational

Funder types

Other

Identifiers

NCT04143997
PRO00036227

Details and patient eligibility

About

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.

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

0 participants in 1 patient group

PPCM with Diastolic Dysfunction & Normal Systolic Function
Description:
The patient population examined will include patients diagnosed with peripartum cardiomyopathy who have diastolic dysfunction and normal systolic function.
Treatment:
Diagnostic Test: A clinical Transthoracic echocardiogram

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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