Registry for collecting health information and biological samples from patients and the general population
Official title: INtermountain Healthcare Biological Samples Collection Project and Investigational REgistry for the On-going Study of Disease Origin, Progression and Treatment (Intermountain INSPIRE Registry)
Run by Intermountain Health Care, Inc. · NCT02450006 · Data updated 2026-11-12
This study is collecting health information and samples from patients with different health conditions and healthy individuals to help with future medical research.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 50000 (estimated) |
| Sponsor | Intermountain Health Care, Inc. Academic / other |
| Locations | 1 site (Murray, Utah) |
| Status | Recruiting |
| Started | April 2015 |
| Main results expected | April 2050 |
| Study ends | April 2050 |
| Registry record updated | April 14, 2026 |
| Trial ID | NCT02450006 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include males and females of any age and ethnicity diagnosed with healthcare-related conditions or disease-free individuals from the general population.
✕Probably not a fit
Patients who are unable or unwilling to provide informed consent or those with conditions that may increase risk or compromise the registry's quality may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The Intermountain INSPIRE Registry is an observational project aimed at gathering biological samples, clinical information, and laboratory data from patients diagnosed with various healthcare-related conditions at Intermountain Healthcare facilities. It also includes data collection from disease-free individuals in the general population. This long-term registry will utilize samples obtained during routine diagnostic procedures and treatments, with the goal of supporting future research projects. Participation requires informed consent, and the collected data will be used for research purposes after appropriate approvals.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of various healthcare conditions and support future research that may lead to improved patient care.
How similar studies have gone: While this registry approach is common, the specific methodology and focus on a broad range of healthcare conditions may provide novel insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Males or females of any age, any ethnicity, diagnosed with any healthcare-related conditions, presenting to an Intermountain Healthcare-affiliated facility or males or females of any age, any ethnicity, with or without any healthcare-related conditions, including disease-free subjects, from a general population that may include unaffected family members * Patient or patient's representative has the ability to understand and sign a written informed consent form, which must be obtained prior to initiation of any study procedures, using a form that is approved by the applicable IRB. Exclusion Criteria: * Inability or refusal of the patient and/or the patient's legally-acceptable representative to provide informed consent for any reason. * Other conditions that in the opinion of the Principal Investigator or Co-Investigator(s) may increase risk to the subject and/or compromise the quality of the registry project.
Where it's running
-
Intermountain Medical Center and Intermountain Clinics
Murray, Utah, United States Recruiting
Study contacts
- Study coordinator: Joseph B Muhlestein, MD
- Email: brent.muhlestein@imail.org
- Phone: 801-507-4701
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.