CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 11 enrolled
Drug / intervention
Microneedle based interstitial fluid collectionprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05546229
NCT05546229N/ACompleted

Interstitial Fluid Collection Validation Study

Cari Health Inc.·observational·Posted Sep 19, 2022·Updated Jun 28, 2023

In Brief

An observational study evaluating Microneedle based interstitial fluid collection for Opioid Use Disorder. Completed, enrolled 11 participants across 1 site.

Detailed Summary

The purpose of this research is to determine if common medications for opioid use disorder (i.e., buprenorphine/naloxone, buprenorphine, methadone) and their metabolites (norbuprenorphine \[a metabolite of buprenorphine\], buprenorphine-3-glucuronide \[B3G; a metabolite in buprenorphine\], ethylidene dimethyl diphenyl pyrrolidine \[EDDP; a metabolite of methadone\]) can be detected in the dermal interstitial fluid (i.e., fluid extracted from the surface of the skin). Additional subjects who are not prescribed or taking any of these medications will be included in this study to act as a comparison group

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2023202420252026
First PostedSep 19, 2022
Enrollment StartSep 14, 2022
Primary CompletionOct 31, 2022
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 3.8 years ago

Interventions

Microneedle based interstitial fluid collectionprocedure

Interstitial fluid will be collected from the skin using microneedles and suction.