- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03900169
Familial Hypercolerstremia as Risk Factor in Stemi Patient Who Underwent Ppci
June 3, 2021 updated by: Amira Harby, Assiut University
Familial Hypercoleresremia as Risk Factor in Stemi Patient Underwent Ppci
Famulial hypercolerstremia as risk factor
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
Familial hypercolerestremia ad risk factor in stemi patient who underwent Ppci
Study Type
Observational
Enrollment (Actual)
2
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
-
-
-
Assiut, Egypt
- Amira harby
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Stemi patient
Description
Inclusion Criteria:
-all patient that underwent Ppci
Exclusion Criteria:
- Previous ischemic patient
- Patient with raised renal chemistry
- Patient for CABG
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 |
---|---|
Stemi patient
Stemi patient who underwent Ppci
|
Lipid profile
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Correlation between familial hypercolerstremia and prognosis of patients in PPCI
Time Frame: One year
|
Correlation between familial hypercolerstremia and prognosis of patients in PPCI
|
One year
|
Correlation between non familial hypercolerstremia and prognosis of patients in PPCI
Time Frame: One year
|
Correlation between non familial hypercolerstremia and prognosis of patients in PPCI
|
One year
|
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 (Actual)
November 1, 2020
Primary Completion (Anticipated)
August 1, 2021
Study Completion (Anticipated)
November 1, 2021
Study Registration Dates
First Submitted
March 25, 2019
First Submitted That Met QC Criteria
March 30, 2019
First Posted (Actual)
April 2, 2019
Study Record Updates
Last Update Posted (Actual)
June 7, 2021
Last Update Submitted That Met QC Criteria
June 3, 2021
Last Verified
June 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Familial hypercolerstremia
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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