Kenota 1 CWS Method Comparison Validation Study

Sponsor

Kenota Inc. (Industry)

Overall Status

Recruiting

CT.gov ID

NCT05702671

Collaborator

(none)

360

Enrollment

Locations

1.7

Anticipated Duration (Months)

120

Patients Per Site

70.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The goal of this Method Comparison Study is to compare total IgE results obtained from at least 360 subjects aged less than 80 years old using four different testing arms comprising three types of samples and two testing methods. The main questions it aims to answer are:

Are the Kenota 1 Devices easy to use by untrained operators at a clinic environment?
Do tIgE results provided by the Kenota 1 Devices match the results provided by the FDA-cleared Phadia ImmunoCAP System?

Subjects will be asked to donate two fingerstick whole blood samples and one venous blood draw.

Condition or Disease	Intervention/Treatment	Phase
Allergy Immunoglobulin E-Mediated Allergic Disorder	Diagnostic Test: Total Immunoglobulin E, Obtained From Fingerstick Sample

Detailed Description

The Method Comparison Study will compare total IgE results obtained from at least 360 subjects aged less than 80 years old using four different testing arms. comprising three types of samples and two testing methods.

Arm (A): Fresh fingerstick whole blood will be collected and tested on Kenota 1 Devices at three CLIA-Waived sites (CWSs).

Arm (B): Venous plasma will be collected at the CWSs and tested on Kenota 1 Devices at the central lab site.

Arm (C): Venous plasma will be collected at the CWSs and tested on Phadia instruments (ImmunoCAP) at the central lab site.

Arm (D): Venous whole blood will be collected at the CWSs and tested on Kenota 1 Devices at the central lab site.

The first method for this study is the Kenota 1 System, which will be used across Three (3) U.S. CWSs. At each CWS, 120 subjects will be recruited and will be asked to donate fingerstick blood and venous blood.

Three (3) untrained operators at each site will be running the freshly collected fingerstick blood samples on the Kenota 1 Devices provided at the site (Testing Arm A). Site operators will also process and store the collected venous blood and venous plasma samples as instructed, and ship them to the central lab for further testing.

The second method for this study involves testing at a Central US Laboratory as a CLIA-regulated laboratory.

At the central lab, at least one trained lab operator will run frozen venous plasma (testing Arm B) and frozen venous whole blood (testing Arm D) collected from all subjects using the Kenota 1 Devices provided at the central lab. As the comparator method, one lab operator will run a second set of frozen plasma samples collected from all subjects on the Phadia ImmunoCAP System (testing Arm C).

The Method Comparison Validation Study is expected to be completed within two months and will be run in conjunction with the Multi-Site Reproducibility Validation Study. All testing will include a daily External Control session on each device used, ensuring the devices are performing as expected.

Study Design

Study Type:

Observational

Anticipated Enrollment :

360 participants

Observational Model:

Cohort

Time Perspective:

Cross-Sectional

Official Title:

Clinical Validation Study of Point of Care Kenota 1 System and Total Immunoglobulin E Test Kit Using the CWS Method Comparison Validation Study

Actual Study Start Date :

Jan 27, 2023

Anticipated Primary Completion Date :

Mar 3, 2023

Anticipated Study Completion Date :

Mar 20, 2023

Outcome Measures

Primary Outcome Measures

Total IgE Value [One day]
Tests performed on the Kenota 1 Devices will provide tIgE values in kU/L for each test. These values will be compared directly with the tIgE results produced by the comparator method, Phadia ImmunoCAP system, which are also in kU/L. The Slope, Intercept and Correlation Coefficient will be calculated and used to determine if overall proportional bias of Kenota 1 fresh fingerstick whole blood is less than 10% compared to the comparator method.

Eligibility Criteria

Criteria

Ages Eligible for Study:

N/A to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Ages <80 years
From all Ethnic/Racial backgrounds

Exclusion Criteria:

Individuals older than 80 years of age
Individuals with skin damage, burns or scars at the site of venipuncture on both arms

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	St. Paul Allergy & Asthma	Saint Paul	Minnesota	United States	55116
2	Allergy Partners of Chapel Hill	Chapel Hill	North Carolina	United States	27514
3	Children's Specialty Group	Virginia Beach	Virginia	United States	23456