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Completed Phase 2 Interventional

Safety and Efficacy of K-134 for the Treatment of Intermittent Claudication

ClinicalTrials.gov ID: NCT00783081

Public ClinicalTrials.gov record NCT00783081. 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 19, 2026, 10:49 AM EDT

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

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of K-134 for the treatment of intermittent claudication.

Study identification

NCT ID
NCT00783081
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kowa Research Institute, Inc.
Industry
Enrollment
387 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
Nov 2008 (Type not available)
Primary completion
Jul 2010 (Actual)
Completion
Jul 2010 (Actual)
Last update posted
Mar 22, 2012

2008 – 2010

United States locations

U.S. sites
30
U.S. states
16
U.S. cities
30
Facility City State ZIP Site status
Not listed Tucson Arizona — —
Not listed Little Rock Arkansas — —
Not listed Beverly Hills California — —
Not listed Los Angeles California — —
Not listed Sacramento California — —
Not listed Santa Rosa California — —
Not listed Vista California — —
Not listed Aurora Colorado — —
Not listed Clearwater Florida — —
Not listed Gulf Breeze Florida — —
Not listed Hialeah Florida — —
Not listed Jacksonville Florida — —
Not listed Pensacola Florida — —
Not listed Sarasota Florida — —
Not listed St. Petersburg Florida — —
Not listed Aurora Illinois — —
Not listed Chicago Illinois — —
Not listed Hinsdale Illinois — —
Not listed Indianapolis Indiana — —
Not listed Auburn Maine — —
Not listed St Louis Missouri — —
Not listed Oklahoma City Oklahoma — —
Not listed Danville Pennsylvania — —
Not listed Warwick Rhode Island — —
Not listed Charleston South Carolina — —
Not listed Amarillo Texas — —
Not listed Houston Texas — —
Not listed Norfolk Virginia — —
Not listed Richmond Virginia — —
Not listed Madison Wisconsin — —

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00783081, 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 Mar 22, 2012 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00783081 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →