Inotrope, Evaluation and Research (INTERPRET) Patient Registry Program

Status: Completed
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The INTERPRET Inotrope Evaluation and Research Patient Registry is a longitudinal, observational study designed to look at the demographics and outcomes of heart failure patients on inotropic therapy administered in the home or infusion suite setting. The data gathered in this registry will provide information on how a patient's quality of life and symptoms change over time while on inotrope therapy, and help healthcare providers to have a better understanding of the benefits and risks associated with bridge-to-treatment and palliative care.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient must be prescribed inotropic treatment (milrinone, dobutamine or dopamine)

• Patient must be referred to Coram for this treatment in an alternate site of care, either home or infusion suite

• Patient must be willing to receive care and comply with the teaching and training necessary to administer treatment

• Patient is age 18 or over

Locations
United States
Alabama
University of Alabama at Birmingham
Birmingham
Illinois
Northwestern University, Bluhm Cardiovascular Institute
Chicago
Kansas
The University of Kansas Medical Center Research Institute
Kansas City
New York
Columbia University Medical Center/Vivian and Seymour Milstein Family Heart Center
New York
Icahn School of Medicine at Mount Sinai
New York
Time Frame
Start Date: 2014-08-25
Completion Date: 2021-09-30
Participants
Target number of participants: 129
Related Therapeutic Areas
Sponsors
Collaborators: Columbia University, Northwestern University, University of Kansas Medical Center, Icahn School of Medicine at Mount Sinai, University of Alabama at Birmingham
Leads: Coram Clinical Trials

This content was sourced from clinicaltrials.gov