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Milky Way Sensor Motion Validation

NCT07228416 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2025-11-14

No results posted yet for this study

Summary

A single arm study of 20 adult volunteers to assess the safety and efficacy of the ivWatch sensors when observing non-infiltrated (normal) tissues at common peripheral IV therapy sites.

Conditions

  • Infiltration of Peripheral IV Therapy

Interventions

DEVICE

ivWatch Model 400

The ivWatch Model 400 monitored tissue at common IV sites over a 24 hour period.

Sponsors & Collaborators

  • ivWatch, LLC

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-12-31
Primary Completion
2026-01-31
Completion
2026-01-31
FDA Device
Yes

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07228416 on ClinicalTrials.gov