- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01759433
Reference Intervals for Sonoclot Analysis in Chinese
December 28, 2013 updated by: Zhenlu Zhang, Wuhan Asia Heart Hospital
Reference Ranges for Sonoclot Analysis in Chinese
The reference intervals for Sonoclot Analysis may be different between Chinese and American.
So far, no reference interval has been established in Chinese for Sonoclot Analysis.
This study is going to establish the first Chinese reference intervals for Sonoclot Analysis and test whether they are different from American reference intervals.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
135
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
-
-
Hubei
-
Wuhan, Hubei, China, 430022
- Wuhan Asia Heart Hospital
-
-
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 to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Chinese healthy adults aged 18 and older
Description
Inclusion Criteria:
- Aged 18 and older
- Han ethnic
Exclusion Criteria:
- Renal dysfunction
- Liver disorders
- Known coagulation disorders
- Patients taking medications in the last month
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The reference intervals for sonoclot analysis in Chinese
Time Frame: 3 month
|
whether Chinese reference intervals are different from Caucasian reference intervals.
|
3 month
|
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
December 1, 2012
Primary Completion (Actual)
March 1, 2013
Study Completion (Actual)
March 1, 2013
Study Registration Dates
First Submitted
November 29, 2012
First Submitted That Met QC Criteria
December 30, 2012
First Posted (Estimate)
January 3, 2013
Study Record Updates
Last Update Posted (Estimate)
December 31, 2013
Last Update Submitted That Met QC Criteria
December 28, 2013
Last Verified
December 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SCWH001
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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