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Recruiting NCT07260799

NCT07260799 Clinical Performance of Capillary Blood Samples Collected Using the Tasso+ Serum Gel Capillary Blood Collection System for Clinical Chemistry Testing of 14 Analytes on an Abbott Alinity Analyzer

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Clinical Trial Summary
NCT ID NCT07260799
Status Recruiting
Phase
Sponsor Tasso Inc.
Condition Serum Analytes
Study Type OBSERVATIONAL
Enrollment 150 participants
Start Date 2025-10-25
Primary Completion 2026-05-31

Trial Parameters

Condition Serum Analytes
Sponsor Tasso Inc.
Study Type OBSERVATIONAL
Phase N/A
Enrollment 150
Sex ALL
Min Age 18 Years
Max Age 85 Years
Start Date 2025-10-25
Completion 2026-05-31
Interventions
Tasso+ Serum Gel Capillary Blood Collection System

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Brief Summary

The purpose of this single-visit study is to demonstrate the performance of capillary blood samples collected with the Tasso+ Serum Gel Capillary Blood Collection System compared to venous reference samples for downstream analyte testing at a clinical laboratory.

Eligibility Criteria

Inclusion Criteria: 1. Adults aged 18-85 years with no previous experience with the Tasso+ lancet 2. Willing and able to provide written informed consent prior to study entry 3. Willing and able to adhere to study assessments, schedule, prohibitions and restrictions as described in the protocol 4. Healthy individuals or patients with abnormal analyte values (verified or likely to be) within intended clinical reference ranges as indicated by standard of care testing and/or past medical history, in the judgement of the investigator Exclusion Criteria: 1. Present with abnormal skin integrity or atypical skin health near/on arm collection sites 2. Mental or physical impairment which would preclude participation in the judgement of the investigator or qualified designee 3. Trained clinical laboratory and healthcare personnel who have worked in the field in the previous 5 years 4. Any condition which, in the opinion of the investigator or delegate, makes the participant unsuitable for this s

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