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PPCM Observational Study (Peripartum Cardiomyopathy)
NCT04234659 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to examine the clinical treatment of patients diagnosed with peripartum cardiomyopathy complicated by cardiogenic shock.
Conditions Studied
Interventions
- DEVICE Clinical placement of a temporary IMPELLA® mechanical circulatory support device.
Study Locations (1)
Wisconsin
- Medical College of Wisconsin — Milwaukee
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2021-01-11 |
| Est. Completion | 2025-08-05 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04234659
The ClinicalTrials.gov registry entry for NCT04234659 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical College of Wisconsin, which has 614 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Cardiogenic Shock appearing as the primary indexed condition, and to 1 intervention — of which Clinical placement of a temporary IMPELLA® mechanical circulatory support device. is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04234659 reports 1 study location spanning 1 distinct geographic area — top geographies include Wisconsin. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04234659 about?
NCT04234659 is a clinical study titled "PPCM Observational Study (Peripartum Cardiomyopathy)". The purpose of this study is to examine the clinical treatment of patients diagnosed with peripartum cardiomyopathy complicated by cardiogenic shock.
What is the current status of trial NCT04234659?
This trial is currently completed. The enrollment target is 150 participants. The study started on 2021-01-11. Estimated completion is 2025-08-05.
What conditions does trial NCT04234659 study?
This clinical trial studies the following conditions: Cardiogenic Shock, Peripartum Cardiomyopathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04234659?
The interventions under investigation include: Clinical placement of a temporary IMPELLA® mechanical circulatory support device. (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04234659?
This trial is sponsored by Medical College of Wisconsin, which has 614 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04234659 being conducted?
This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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