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Completed Phase 4 Interventional Results available

Evaluation of Cilostazol in Combination With L-Carnitine

ClinicalTrials.gov ID: NCT00822172

Public ClinicalTrials.gov record NCT00822172. 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 May 6, 2026, 8:49 AM EDT

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

Official title

Evaluation of Cilostazol in Combination With L-Carnitine in Subjects With Intermittent Claudication

Study identification

NCT ID
NCT00822172
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Colorado Prevention Center
Other
Enrollment
164 participants

Conditions and interventions

Interventions

  • Levocarnitine tartrate Dietary Supplement
  • cilostazol Drug

Dietary Supplement · Drug

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
Aug 31, 2008
Primary completion
Oct 31, 2010
Completion
Nov 30, 2010
Last update posted
Nov 28, 2019

2008 – 2010

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Internal Medicine Physicians Associates Phoenix Arizona 85006
Tatum Ridge Internal Medicine Phoenix Arizona 85032
Central Arkansas Veteran's Healthcare System Little Rock Arkansas 72205
VA Palo Alto Health Care System Palo Alto California 94304
University of California at Davis Vascular Center Sacramento California 95817
Sacramento Heart and Vascular Research Center Sacramento California 95825
Apex Research Institute Santa Ana California 92705
Aurora Denver Cardiology Associates Aurora Colorado 80012
Aurora Denver Cardiology Associates Denver Colorado 80218
Pensacola Research Consultants, Inc. Pensacola Florida 32504
DMI Healthcare Group, Inc. Pinellas Park Florida 33782
Meridian Research St. Petersburg Florida 33709
Ochsner Medical Center New Orleans Louisiana 70121
HPV Heart, PA Columbia Maryland 21044
University of Massachusetts Medical Center Worcester Massachusetts 01605
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
University of Rochester Medical Center Rochester New York 14623
Durham VA-Medical Center Durham North Carolina 27705
Radiant Research, Inc Columbus Ohio 43212
Jobst Vascular Center Toledo Ohio 43606
Peripheral Vascular Associates San Antonio Texas 78205
Clinical Trials of Texas, Inc. San Antonio Texas 78229
Radiant Research- Salt Lake City Salt Lake City Utah 84107
Beloit Clinic Research Office Beloit Wisconsin 53511

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00822172, 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 Nov 28, 2019 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00822172 live on ClinicalTrials.gov.

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