Precision Medicine for Dilated Cardiomyopathy-Cardiac Magnetic Resonance to Identify Early Family Phenotypes

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Study is an ancillary study from the parent study, DCM Precision Medicine Study. The rationale for the DCM-CMR study is to leverage cardiac magnetic resonance (CMR) imaging to detect earliest findings of DCM in the at-risk family members enrolled into the parent study.

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

• The FDR's proband was enrolled in the DCM Precision Medicine Study at 1 of 9 participating sites, or exceptions granted by study PI.

• The FDR's proband has had one or more variants identified, including P, LP and VUS.

• The FDR is able report to one of the participating sites for study enrollment.

• The FDR has no current contraindication for CMR (glomerular filtration rate (GFR) \<30 mL/min/1.73 m2, non-compatible device implant, or allergy to gadolinium contrast).

• The FDR has had no prior heart transplant.

• The FDR is ≥18 years of age.

• All races/ethnicity

• Ability to give informed consent.

• Ability to communicate in English.

⁃ Subject is not pregnant (CMR may be conducted 3-6 months post delivery)

⁃ Willingness to participate in a family-based study (subject willing to interact with OSU).

Locations
United States
Ohio
The Ohio State University
RECRUITING
Columbus
Contact Information
Primary
Principal Investigator
DCM.Research@osumc.edu
1-614-688-1388
Backup
Clinical Research Manager
DCM.Research@osumc.edu
1-614-688-9815
Time Frame
Start Date: 2021-04-01
Estimated Completion Date: 2026-04
Participants
Target number of participants: 650
Sponsors
Collaborators: National Heart, Lung, and Blood Institute (NHLBI)
Leads: Ohio State University

This content was sourced from clinicaltrials.gov