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Carbon Monoxide Blood and DNA Biorepository

Carbon Monoxide Blood and DNA Repository

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01758653
Enrollment
300
Registered
2013-01-01
Start date
2012-02-29
Completion date
2032-12-31
Last updated
2023-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carbon Monoxide Poisoning

Keywords

CO poisoning

Brief summary

The purpose of this biorepository is to collect blood from patients at the time of CO poisoning and at follow-up visits months to years later. These samples can be used in the future to learn more about how CO damages the heart and brain and whether blood tests could predict which patients will have problems after CO poisoning.

Detailed description

The investigators propose to establish a biorepository for storage of serum, plasma, and DNA collected from patients with carbon monoxide (CO) poisoning. Participants will also be evaluated for clinical outcome. The biorepository will include serum and plasma from CO-poisoned patients drawn at the time of injury as well as from blood drawn at clinical follow-up visits. The biorepository will also bank DNA from these participants. These specimens can be analyzed in the future to elucidate potential inflammatory and immunological mechanisms that cause brain and heart damage and identify possible biological and genetic predictors of poor outcome.

Interventions

There is no study-related intervention.

Sponsors

Intermountain Health Care, Inc.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Symptomatic carbon monoxide poisoning (headache, nausea, vomiting, dizziness, fatigue, muscle aches, slowed mentation, confusion, loss of consciousness, etc.). 2. Documented exposure to carbon monoxide and no other reasonable explanation for their signs and symptoms.

Exclusion criteria

1. Pregnancy 2. Age \< 18 years 3. Unable to obtain informed consent 4. Subjects who, in the opinion of the investigator, are unable to comply with the requirements of the study or are unsuitable for any reason. The investigator and the Sponsor, prior to enrolling the subject on a case-by-case basis, must approve and document any waiver of these inclusion and

Design outcomes

Primary

MeasureTime frameDescription
Biorepository for serum and plasmaWithin 24 hours of CO PoisoningSerum and plasma from blood collected within 24 hours of acute CO poisoning

Secondary

MeasureTime frameDescription
Serum and plasma (sub-acute)4 weeks to 4 months after CO poisoningSerum and plasma collected 4 weeks to 4 months after poisoning
DNA Sequestration24 hours to 12 months after CO poisoningDNA sequestered from blood drawn up to 1 year from CO poisoning
Serum and plasma (long-term)4 months to 12 months after CO poisoningSerum and plasma collected 4 months to 12 months after poisoning

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026