- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01548274
Impact of Sarpogrelate in the Function of Endothelial Progenitor Cells
March 5, 2012 updated by: Keiko Naruse, Aichi Gakuin University
The purpose of this study is to evaluate the effects of Sarpogrelate in endothelial progenitor cells of patients with atherosclerosis.
Study Overview
Detailed Description
Endothelial progenitor cells play an important role in vasculogenesis and vascular repair.
Sarpogrelate, a inhibitor of HT2A, is used an an anti-platelet drug, however, a direct effect in vascular cells is supposed.
Study Type
Interventional
Enrollment (Anticipated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Aichi
-
Nagoya, Aichi, Japan, 464-8651
- Recruiting
- Aichi-Gakuin University
-
Contact:
- Keiko Naruse, M.D., Ph.D.
- Phone Number: 5369 +81-52-759-2111
- Email: narusek@dpc.agu.ac.jp
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with atherosclerosis
Exclusion Criteria:
- Patients with high risk of bleeding
- Patients with pregnancy
- Patients with allergic reaction of Salpogrelate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The number and function of endothelial progenitor cells
Time Frame: 3 months
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2010
Primary Completion (ANTICIPATED)
October 1, 2012
Study Completion (ANTICIPATED)
October 1, 2012
Study Registration Dates
First Submitted
March 5, 2012
First Submitted That Met QC Criteria
March 5, 2012
First Posted (ESTIMATE)
March 8, 2012
Study Record Updates
Last Update Posted (ESTIMATE)
March 8, 2012
Last Update Submitted That Met QC Criteria
March 5, 2012
Last Verified
March 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Arteriosclerosis
- Arterial Occlusive Diseases
- Atherosclerosis
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Fibrinolytic Agents
- Fibrin Modulating Agents
- Platelet Aggregation Inhibitors
- Serotonin Agents
- Serotonin Antagonists
- Sarpogrelate
Other Study ID Numbers
- AGU-65
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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