Active — Not RecruitingNot Applicable

Database Registry of the Intermountain Heart Collaborative Study

United States30,000 participantsStarted 1994-10

Plain-language summary

The purpose of the registry is to collect and analyze clinical and laboratory data and tissue samples from patients who are diagnosed with any type of heart disease and to collect the same information and samples from healthy controls in participating Intermountain Healthcare facilities.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. The patient (male or non-pregnant female) must be \> 18 years of age.
✓. The patient or legally authorized representative must sign a written informed consent, prior to the procedure, using a form that is approved by the local Institutional Review Board.

Exclusion criteria

✕. Neither patient nor patient representative understands spoken English.
✕. Neither patient nor the patient's personal representative is willing to give written consent for participation.
✕. Healthy control patients must sign their own consent document.

What they're measuring

Outcome Risk

Timeframe: 30 years

Trial details

NCT IDNCT00406185

SponsorIntermountain Health Care, Inc.

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-03

View on ClinicalTrials.gov More Coronary Artery Disease trials