- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03217890
the Relationship Between Cleft Lip and / or Palate (Different Types) and ABO Blood Groups.
July 12, 2017 updated by: Mostafa medhat helmy, Cairo University
Distribution Of ABO Blood Groups In Relation To Cleft Lip And/or Palate .
Direct benefit of the research to assess the relationship between cleft lip and / or palate (different types) and ABO blood groups.
Study Overview
Status
Unknown
Conditions
Detailed Description
376 Egyptian cleft lip and/or palate patients ( age ranged from 2 days to 15 years ) With no syndrome.
Blood group from records will be collected an d then assess the relationship between cleft lip and / or palate (different types) and ABO blood groups.
Study Type
Observational
Enrollment (Anticipated)
376
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
2 days to 15 years (CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
376 Egyptian cleft lip and/or palate patients (Age ranged from 2 days to 15 years ) With no syndrome .
Description
Inclusion Criteria:
- Egyptian Patients with cleft or/and palate
- The children's age ranged between 2 days and 15 years.
Exclusion Criteria:
- syndromic patients
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 |
---|---|---|
Distribution of ABO blood group in relation to different types of cleft lip and/or palate .
Time Frame: 6 months
|
ABO blood group
|
6 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 (ANTICIPATED)
August 1, 2017
Primary Completion (ANTICIPATED)
August 1, 2017
Study Completion (ANTICIPATED)
August 1, 2017
Study Registration Dates
First Submitted
July 11, 2017
First Submitted That Met QC Criteria
July 12, 2017
First Posted (ACTUAL)
July 14, 2017
Study Record Updates
Last Update Posted (ACTUAL)
July 14, 2017
Last Update Submitted That Met QC Criteria
July 12, 2017
Last Verified
July 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CEBC-CU-2017-07-18
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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