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Creation of a Multicenter National Registry for Peripartum Cardiomyopathy.
Sponsor: Federico II University
Summary
Peripartum cardiomyopathy (PPCM) is a rare, severe and potentially life-threatening disorder of largely unknown etiology and pathophysiology, with unexplained geographical differences and heterogeneous presentation. Investigators hypothesize that a network-based multidisciplinary strategy integrating clinical and molecular phenotyping of PPCM patients might anticipate diagnosis, optimize treatments, and identify novel mechanisms to achieve the unmet goal of personalized medicine.
Official title: Creation of a Multicenter National Registry for Peripartum Cardiomyopathy: a Wide, Multidisciplinary and Translational Perspective to Achieve Personalized Medicine for a Rare Disease in Women
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
40
Start Date
2024-02-21
Completion Date
2026-05-19
Last Updated
2024-03-21
Healthy Volunteers
Yes
Conditions
Interventions
Molecular and genetic screening
Molecular and genetic screening
Locations (1)
Federico II University Hospital
Naples, Italy