Viewing Study NCT00991367


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Study NCT ID: NCT00991367
Status: COMPLETED
Last Update Posted: 2010-12-08
First Post: 2009-10-07
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: CICATRIX in the Treatment of Recent Post-surgical Scars
Sponsor: Catalysis SL
Organization:

Study Overview

Official Title: Efficacy of CICATRIX (Asian Gotu Kola or Pennywort) in the Treatment of Recent Post-surgical Scars
Status: COMPLETED
Status Verified Date: 2010-12
Last Known Status: None
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 the study is to assess the efficacy of CICATRIX (Asian Gotu Kola or Pennywort) usage in the treatment of recent post-surgical scars. The duration of this double-blind placebo controlled phase 3 clinical trial will be 4 weeks. The estimated number of persons to be recruited and randomized for the study is 90.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
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?: