Viewing Study NCT01736969


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Study NCT ID: NCT01736969
Status: UNKNOWN
Last Update Posted: 2012-12-03
First Post: 2012-10-12
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Substantial Equivalence Study of RD04723 and Predicate Device
Sponsor: Oculus Innovative Sciences, Inc.
Organization:

Study Overview

Official Title: Microcyn Scar Management HydroGel, K103163 vs. Kelo-coteĀ® Scar Gel for the Management of Hypertrophic or Keloid Scars
Status: UNKNOWN
Status Verified Date: 2012-11
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine whether a developmental formulation is substantially equivalent to the predicate device in the treatment of hypertrophic and keloid scars.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: