Specimen Stability Study

NCT ID: NCT01846884

Last Updated: 2013-05-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

124 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-11-30

Study Completion Date

2013-05-31

Brief Summary

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To collect and process urine samples from critically ill subjects for use in assessing the effects of various urine sample freezing and storage conditions on biomarker test results.

Detailed Description

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Conditions

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Acute Kidney Injury

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

1. Males and females 21 years of age or older
2. Subjects must be enrolled (first study-specific sample collection) within 24 hours of ICU admission

* Subjects enrolled from ED or Floor must be admitted to the ICU within 24 hours of enrollment
* Subjects enrolled in the ICU must have been admitted to the ICU or transferred into the study ICU from another ICU no more than 24 hours prior to enrollment
3. Expected to remain in the ICU for at least 48 hours after enrollment
4. Use of indwelling urinary catheter as standard care expected for at least 48 hours after enrollment
5. Subject (or authorized representative)able and willing to provide written informed consent for study participation

Exclusion Criteria

1. Special populations including children, pregnant women, and prisoners
2. Previous renal transplantation
3. Already receiving dialysis (either acute or chronic) or in imminent need of dialysis at the time of enrollment
4. Known infection with human immunodeficiency virus (HIV) or active hepatitis (acute or chronic)
5. Subjects with a history of chronic kidney disease (CKD) without a baseline serum creatinine value (baseline within 6 months of enrollment)
6. Previously provided a urine sample and enrolled in this study
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Astute Medical, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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La Mesa, California, United States

Site Status

Honolulu, Hawaii, United States

Site Status

Idaho Falls, Idaho, United States

Site Status

Las Vegas, Nevada, United States

Site Status

Port Jefferson, New York, United States

Site Status

Greenville, North Carolina, United States

Site Status

Countries

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United States

References

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Hoste EA, McCullough PA, Kashani K, Chawla LS, Joannidis M, Shaw AD, Feldkamp T, Uettwiller-Geiger DL, McCarthy P, Shi J, Walker MG, Kellum JA; Sapphire Investigators. Derivation and validation of cutoffs for clinical use of cell cycle arrest biomarkers. Nephrol Dial Transplant. 2014 Nov;29(11):2054-61. doi: 10.1093/ndt/gfu292. Epub 2014 Sep 18.

Reference Type DERIVED
PMID: 25237065 (View on PubMed)

Other Identifiers

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Opal

Identifier Type: -

Identifier Source: org_study_id

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