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Clinical Performance of Capillary Blood Samples Collected Using the Tasso+ Serum Gel Capil

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.

Condition(s)Serum Analytes
StatusRecruiting
Study typeObservational
SummaryThe 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.
Who can participateInclusion 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 labo
Ages18 Years to 85 Years
SexAll
Accepts healthy volunteersYes
Lead sponsorTasso Inc.
LocationsAtlantis, Florida, United States
Start date2025-10-25
NCT IDNCT07260799
Official listinghttps://clinicaltrials.gov/study/NCT07260799

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