CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 65 enrolled
Drug / intervention
Microcyn +1 moredrug
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/NCT02001558
NCT02001558Phase 4Completed
CompareCT.gov

A Six Month Randomized Open-Label Trial of Pressure Ulcer Healing With Microcyn® Skin and Wound Care With Preservatives Versus Sterile Saline in Adult Spinal Cord Injury Subjects

University of Alabama at Birmingham·interventional·Posted Dec 5, 2013·Updated Nov 6, 2018

In Brief

A Phase 4 clinical trial evaluating Microcyn and Sterile saline for Pressure Ulcer and Spinal Cord Injuries. Completed, enrolled 65 participants across 1 site.

Detailed Summary

The purpose of this study is to test how well Microcyn™ works on Stage 3 and Stage 4 pressure ulcers compared to sterile saline among persons with spinal cord injury.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPressure Ulcer, Spinal Cord Injuries
CountriesUnited States
CollaboratorsOculus Innovative Sciences, Inc.

Timeline

Phase 4CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedDec 5, 2013
Enrollment StartMar 1, 2013
Primary CompletionAug 1, 2017
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 12.6 years ago

Interventions

Microcyndrug

Microcyn is liberally sprayed on wound and permitted to remain on wound which will then be dressed with gauze that is moistened with Microcyn twice daily for the earlier of total wound closure or Week 24

Sterile salineother

Sterile saline is liberally sprayed on wound and permitted to remain on wound which will then be dressed with gauze that is moistened with sterile saline twice daily for the earlier of total wound closure or Week 24