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Completed No phase listed Observational

Restore EF Observational Study

ClinicalTrials.gov ID: NCT04648306

Public ClinicalTrials.gov record NCT04648306. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 9:25 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Restore EF Observational Study (in High-risk PCI)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A multi-center, prospective, observational, non-interventional single arm, study of the intermediate-term clinical outcomes collected from electronic health records of high-risk patients which have previously undergone standard of care prophylactic Impella support for a non-emergent percutaneous coronary intervention (PCI).

Study identification

NCT ID
NCT04648306
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Abiomed Inc.
Industry
Enrollment
406 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 1, 2019 (Actual)
Primary completion
May 31, 2021 (Actual)
Completion
Sep 30, 2021 (Actual)
Last update posted
Dec 14, 2021

2019 – 2021

United States locations

U.S. sites
21
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
St. Joseph's Medical Center Phoenix Arizona 85016 —
Tucson Medical Center Tucson Arizona 85719 —
Washington Regional Medical Center Fayetteville Arkansas 72703 —
Arkansas Cardiology P.A. North Little Rock Arkansas 72117 —
Northwest Medical Center Springdale Arkansas 72764 —
Loma Linda University Medical Loma Linda California 92354 —
UCSD Medical Center San Diego California 92093 —
Advent Health Daytona Beach Florida 32117 —
NorthShore University HealthSystem Skokie Illinois 60076 —
Genesis Medical Center Davenport Iowa 52803 —
Baptist Healthcare System Lexington Kentucky 40503 —
Lafayette General Medical Center Houma Louisiana 70360 —
Mercy Hospital Coon Rapids Minnesota 55433 —
St. Cloud Hospital Saint Cloud Minnesota 56303 —
NYU Langone Medical Center New York New York 10016 —
Vidant Medical Center Greenville North Carolina 28275 —
Christ Hospital Cincinnati Ohio 45219 —
Providence Portland Medical Center Portland Oregon 97213 —
Presbyterian Hospital Dallas Arlington Texas 76011 —
Kingwood Medical Center Kingwood Texas 77339 —
Sentara Healthcare Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04648306, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 14, 2021 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04648306 live on ClinicalTrials.gov.

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