Clinical Trials in the USA / NCT07908056
Starting soon
Observational
Evaluate Precision of the Test for Lactate in Capillary Whole Blood Specimens Using the i-STAT CG4+ Cartridge With the i-STAT 1 Analyzer
NCT07908056 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Lactate
Investigational drug(s) / intervention(s)
Fingerstick capillary blood draw
Fingerstick capillary blood draw: Fingerstick capillary blood draw
Study summary
Assess precision of the i-STAT lactate test with the i-STAT CG4+ cartridge on the i-STAT 1 analyzer using two (2) separate capillary blood specimens.
Eligibility
Inclusion Criteria:
Subject Inclusion Criteria
1. Signed and dated consent form (waiver/alteration of consent, waiver of documentation of consent may be acceptable, per IRB)
2. ≥ 18 years of age
Exclusion Criteria:
Subject Exclusion Criteria
1\. Previous enrollment in this study
Primary outcome measure(s)
- Precision across the reportable range for lactate — Through study completion, an average of 1 year
The primary outcome measure is to assess the precision across the lactate reportable range for the i-STAT lactate test using the i-STAT CG4+ cartridge on the i-STAT 1 analyzer.
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| Hackensack University Medical Center | Hackensack | New Jersey | |
| Penn State Health Milton S. Hershey Medical Center (Hershey) | Hershey | Pennsylvania | |
| Medical College of Wisconsin | Milwaukee | Wisconsin |
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07908056 on ClinicalTrials.gov ↗ ← All trials in the USA