Viewing Study NCT00059657



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Last Modification Date: 2024-10-26 @ 9:08 AM
Study NCT ID: NCT00059657
Status: COMPLETED
Last Update Posted: 2006-05-19
First Post: 2003-04-29

Brief Title: EfficacySafety of Ecraprost in Lipid Emulsion for Treatment of Critical Leg Ischemia Due to Peripheral Arterial Disease
Sponsor: Mitsubishi Tanabe Pharma Corporation
Organization: Mitsubishi Tanabe Pharma Corporation

Study Overview

Official Title: A Double-Blind Randomized Placebo-Controlled Study to Assess the Efficacy and Safety of CirculaseTM in Conjunction With Peripheral Revascularization for the Treatment of Critical Leg Ischemia
Status: COMPLETED
Status Verified Date: 2006-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Ecraprost in lipid emulsion is being developed for the treatment of Critical leg ischemia CLI which is the most severe form of peripheral arterial disease PAD This trial is designed to assess the efficacy and safety of the drug in the treatment of CLI
Detailed Description: None

Study Oversight

Has Oversight DMC: None
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?: None