CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 26 enrolled
Drug / intervention
GLYC-101 Gel (0.1%) +2 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/NCT00792688
NCT00792688Phase 2Completed

Double-Blind, Randomized, Placebo-Controlled Phase 2 Study to Investigate the Safety and Efficacy of 0.1% and 1.0% Topically Applied GLYC-101, Compared to Placebo, in Patients Undergoing Carbon Dioxide Laser Skin Resurfacing of the Lower Eyelids.

TR Therapeutics·interventional·Posted Nov 18, 2008·Updated Oct 28, 2021

In Brief

A Phase 2 clinical trial evaluating GLYC-101 Gel (0.1%), GLYC-101 Gel (1.0%), and 1 other intervention for Wounds. Completed, enrolled 26 participants across 1 site.

Detailed Summary

The primary objectives of this study are to evaluate safety and efficacy of topically applied Glucoprime gel (GLYC-101, 0.1% and GLYC-101, 1.0%) in promoting wound healing in cosmetic surgery patients undergoing Carbon Dioxide Laser Skin Resurfacing (CO2 LSR) of the lower eyelids. The study will observe the effects of the topical agent over the course of 1 month following the initial treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsWounds
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedNov 18, 2008
Enrollment StartOct 1, 2008
Primary CompletionJan 1, 2010
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 17.6 years ago

Interventions

GLYC-101 Gel (0.1%)drug

Topical administration to the laser-ablated area on days 1 (day of laser ablation), 2, 3, 4, and 5.

GLYC-101 Gel (1.0%)drug

Topical administration to the laser-ablated area on days 1 (day of laser ablation), 2, 3, 4, and 5.

GLYC-101 Placebodrug

Topical administration to the laser-ablated area on days 1 (day of laser ablation), 2, 3, 4, and 5.