CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled
Drug / intervention
MolecuLight i:X Imaging Devicedevice
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/NCT02682069
NCT02682069N/ACompleted

A Prospective, Single-blind Evaluation of the Positive Predictive Value (PPV) of the MolecuLight i:X(TM) Imaging Device to Predict the Presence of Bacteria in Chronic Wounds

MolecuLight Inc.·interventional·Posted Feb 15, 2016·Updated Feb 26, 2020

In Brief

A clinical study evaluating MolecuLight i:X Imaging Device for Wounds. Completed, enrolled 30 participants.

Detailed Summary

This is a non-randomized evaluation for which 50 patients will be imaged at the Southwest Regional Wound Care Center, Lubbock, Texas, who present with a chronic wound and are receiving standard treatment. The MolecuLight i:X Imaging Device will be used as an adjunctive tool in the assessment of the wound and will be used to guide the targeted sampling of a wound (punch biopsy method).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsWounds
Countries--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 15, 2016
Enrollment StartFeb 1, 2016
Primary CompletionJan 5, 2017
Study CompletionAug 30, 2017
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 10.4 years ago

Interventions

MolecuLight i:X Imaging Devicedevice

The intended use of the device is to assist clinicians during care and management of patients with chronic wounds by screening for the presence of potentially harmful bacteria levels. The device will be used as part of the current clinical wound assessment process which may include examination for characteristic signs and symptoms of infection. The device can capture and document either an image or video of the chronic wound where the presence of florescent bacteria appears under violet light illumination. This information can be used to guide a clinician to inspect, sample, debride or further evaluate areas within or around a wound where fluorescent bacteria are present.