- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02720861
Prevalence of Genetic Polymporphism on RNF213 rs112735431 Gene in Non-cardioemboli Ischemic Cerebrovascular Disease
March 25, 2016 updated by: Suporn Travanichakul, MD., Chulalongkorn University
Prevalence of Genetic Polymporphism on RNF213 rs112735431 Gene in Non-cardioemboli Ischemic Cerebrovascular Disease: A Cross-sectional Study in Thai Patients
To explore the prevalence of genetic polymorphism on RNF213 rs112735431 gene in non-cardioembolic ischemic cerebrovascular disease in Thai patients.
Study Overview
Detailed Description
This is an cross-sectional observational study in Chulalongkorn hospital, to determine the prevalence of genetic polymorphism on RNF213 rs112735431 gene in non-cardioembolic ischemic cerebrovascular disease.
Patients who are potentially eligible for study participation will be identified through a chart review of patients who were admitted in Chulalongkorn Hospital for acute ischemic stroke treatment.
Study Type
Observational
Enrollment (Anticipated)
200
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
-
-
-
Bangkok, Thailand, 10330
- Recruiting
- Suporn Travanichakul
-
Contact:
- Suporn Travanichakul, MD
- Phone Number: 0858054513
- Email: stravanichakul@yahoo.com
-
Principal Investigator:
- Aurauma Chutinet, MD
-
Principal Investigator:
- Nijasri Charnnarong, MD
-
Principal Investigator:
- Thiti Snabboon, MD
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Acute ischemic stroke patients of Chulalongkorn hospital
Description
Inclusion Criteria:
- Nationality in Thailand
- Age equal or more than 18 years
- Clinical and imaging diagnosis of acute ischemic stroke
- Patient consent to participate in the research
Exclusion Criteria:
- High risk for cardioembolic stroke by TOAST classification
- Contraindication for venipuncture
- Pregnancy or breast feeding patient
- History of head and neck radiation
- Down's syndrome
- Marfan syndrome
- Autoimmune disease such as SLE
- Ongoing malignancy or remission of malignancy less than 1year
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
non embolic ischemic stroke
acute ischemic stroke from atherosclerosis or lacunar stroke
|
withdraw 3m blood from vein only once during the whole design to analyse on DNA sequencing on RNF213 rs112735431 Gene
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of Participants With RNF213 rs112735431 Gene polymorphism
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Suporn Travanichakul, MD, Chulalongkorn University
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
March 1, 2015
Primary Completion (Actual)
March 1, 2016
Study Completion (Anticipated)
June 1, 2016
Study Registration Dates
First Submitted
March 15, 2016
First Submitted That Met QC Criteria
March 25, 2016
First Posted (Estimate)
March 28, 2016
Study Record Updates
Last Update Posted (Estimate)
March 28, 2016
Last Update Submitted That Met QC Criteria
March 25, 2016
Last Verified
March 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- COA No.282/2015
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Not Share
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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