A Multi-Center Study of A New Method of Sweat Testing: The CF Quantum® Sweat Test
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cystic Fibrosis
- Sponsor
- Polychrome Medical, Inc.
- Enrollment
- 55
- Locations
- 6
- Primary Endpoint
- Diagnostic sensitivity and specificity (true positive rate and the false negative rate to measure chloride in the sweat sample) of the new sweat test device compared to the standard-of-care sweat test device
- Status
- Terminated
- Last Updated
- 7 years ago
Overview
Brief Summary
This is an observational comparative study to compare the standard-of-care methods for sweat testing used to support diagnosing cystic fibrosis (CF) against a new method of sweat testing called the CF Quantum Sweat Test System. The results of the new device in this study are for comparison ONLY and will NOT be used to diagnose, treat or mitigate the subject's condition.
Detailed Description
The primary objective is to evaluate the diagnostic accuracy of a new sweat test method in both normal individuals and individuals with CF or cystic fibrosis related metabolic syndrome (CRMS). Subject participation is for one day and duration of study for each subject is one day. No follow-up will be required. Number of subjects; 300 split evenly between subjects with previously diagnosed CF or CRMS (cystic fibrosis related metabolic syndrome) and subjects referred to the sweat test lab for clinical reasons. Number of sites = 6, U of WI-Madison, U of WI-Milwaukee, U of MI-Ann Arbor, Dayton Children's Hospital (OH), U of MN, and Children's of Alabama. Primary endpoints: * Clinical and analytical sensitivity of the new test method * Clinical and analytical sensitivity of the standard-of-care methods Statistics Sensitivity and specificity will be calculated and reported along with the corresponding 95% confidence intervals. Bias assessment will be conducted according to the Clinical and Laboratory Standards Institute (CLSI) guidelines for method comparison and bias estimation. Pearson's correlation analysis will be conducted to test for adequate range of the replicate values for the new test method.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients referred to the sweat test lab on a clinical basis.
- •Infants who require a sweat test as follow-up to an abnormal CF screening test.
- •Patients who have already been diagnosed with CF or CRMS.
- •Written informed consent (and assent when applicable) obtained from subject or subject's legal representative.
Exclusion Criteria
- •Patient is receiving oxygen by open delivery.
- •Infants less than 48 hours of age.
- •Diffuse inflammation or rash on the collection site.
- •Patients who have had a reaction to a prior iontophoretic sweat test procedure.
- •Arm is too small for both the new and conventional sweat test.
Outcomes
Primary Outcomes
Diagnostic sensitivity and specificity (true positive rate and the false negative rate to measure chloride in the sweat sample) of the new sweat test device compared to the standard-of-care sweat test device
Time Frame: Day 1
Secondary Outcomes
- Compare the sweat test's "quantity not sufficient" (QNS) rate of the new device to the standard-of-care device.(Day 1)