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Completed No phase listed Observational Results available

REducing 30-day ADMIssions in posT-discharge Subjects (READMIT)

ClinicalTrials.gov ID: NCT01574144

Public ClinicalTrials.gov record NCT01574144. 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 4, 2026, 1:34 PM EDT

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

Official title

Observational Study of Reducing 30-day Admissions in Post-discharge Subjects

Brief summary

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

The purpose of this observational study is to collect and characterize multiple physiologic data from a broad subset of subjects with acute heart failure (HF) Changes in physiologic data are expected to correlate with 30-day readmission rates in this population

Study identification

NCT ID
NCT01574144
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
70 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
Apr 2012 (Type not available)
Primary completion
Apr 2013 (Actual)
Completion
Aug 2013 (Actual)
Last update posted
Dec 30, 2022

2012 – 2013

United States locations

U.S. sites
7
U.S. states
7
U.S. cities
7
Facility City State ZIP Site status
Scripps Green Hospital La Jolla California 92037 —
Bay Area Cardiology Tampa Florida 33511-5908 —
United Heart and Cardiovascular Saint Paul Minnesota 55102-2568 —
Morristown Memorial Hospital Morristown New Jersey 07962 —
Mohawk Valley Heart Institute Utica New York 13501-5930 —
University of Cincinnati Cincinnati Ohio 45219-2364 —
Vanderbilt University Nashville Tennessee 37232 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01574144, 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 30, 2022 · Synced Oct 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01574144 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →