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Terminated Phase 3 Interventional

Efficacy/Safety of Ecraprost in Lipid Emulsion for Treatment of Critical Leg Ischemia Due to Peripheral Arterial Disease

ClinicalTrials.gov ID: NCT00059644

Public ClinicalTrials.gov record NCT00059644. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 5:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Randomized, Placebo-Controlled Study to Assess the Efficacy and Safety of CirculaseTM for the Treatment of Critical Leg Ischemia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00059644
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tanabe Pharma Corporation
Industry
Enrollment
560 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2001 (Type not available)
Primary completion
Not listed
Completion
Jun 2004 (Type not available)
Last update posted
Jun 24, 2005

2001 – 2004

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Tucson Arizona — —
Not listed Glendale California — —
Not listed Los Angeles California — —
Not listed Pasadena California — —
Not listed San Francisco California — —
Not listed Pensacola Florida — —
Not listed Springfield Illinois — —
Not listed Indianapolis Indiana — —
Not listed New Orleans Louisiana — —
Not listed Royal Oak Michigan — —
Not listed Biloxi Mississippi — —
Not listed Kansas City Missouri — —
Not listed Henderson Nevada — —
Not listed West Caldwell New Jersey — —
Not listed New York New York — —
Not listed Charlotte North Carolina — —
Not listed Portland Oregon — —
Not listed San Antonio Texas — —
Not listed Tacoma Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00059644, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 24, 2005 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00059644 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →