ALT Routinely Recorded Remotely: A Comparator Study of Liver Function Tests Using the Tasso+ to Venipuncture.
Status unconfirmed
Conditions studied: Elevated Alanine Transaminase (ALT)
In brief
A direct comparison study of blood samples collected using the Tasso+ device and venous blood samples in patients with elevated alanine transaminase (ALT).
Key facts
- Study ID
- NCT05259618
- Run by
- Tasso Inc.
- People needed
- 80
- Starts
- 2021-02-16
- Expected to finish
- 2022-11-01
- Last updated by the study team
- 2022-02-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subject must be willing and able to provide written informed consent prior to study entry
- Subject is ≥ 18 years of age.
- Subject must meet the following criterion:
- known recent history of liver function abnormality and requiring follow-up Liver tests (including ALT>3XULN)
- Subject must be willing and able to adhere to the assessments, study schedule, prohibitions and restrictions as described in the protocol.
- Patients may be on any treatment / therapeutic clinical trial as indicated by treating physician
You may not qualify if…
- Pregnant or nursing female by self-report.
- Presents with abnormal skin integrity or atypical skin health within the areas to be tested (upper shoulders).
- Subjects who have applied lotion to the skin on the shoulder the day of the visit.
- Patients with hepatic encephalopathy
- Vulnerable populations (children, prisoners, pregnant women, participants with diminished decision-making capacity, illiterate populations, educationally disadvantaged populations).
Where it is running
- Memorial Sloan Kettering Cancer Center — New York, New York, United States (enrolling)
- EvergreenHealth Research — Kirkland, Washington, United States (enrolling)
- University of Colorado Anschutz Medical Campus — Aurora, Colorado, United States
Full record on ClinicalTrials.gov
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