Microneedle-based ISF Sampling Technique

Study acronym: MIST
StatusNot Yet Recruiting
PhaseNot applicable
Started

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Record History

  1. Re-verified, no change to tracked fields
  2. Study First Submitted
This clinical investigation aims to evaluate the performance and safety of the PELSA system, a hollow microneedle-based medical device designed for the collection of dermal interstitial fluid (dISF) from human skin. Healthy adult volunteers will undergo a single dISF sampling session using the PELSA system. The primary objective is to assess the proportion of participants from whom at least 1 µL of dISF can be successfully collected during one sampling session. Device safety and tolerability will also be evaluated, including the occurrence of adverse events, participant-reported pain, and local skin reactions. Exploratory assessments may include glucose detection and proteomic analysis of collected dISF samples.
Trial Details
NCT Number NCT07882225
Lead Sponsor Ascilion AB
Collaborators: Charite University, Berlin, Germany
Conditions
(from sponsor)
No Condition, Healthy Individuals
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov