- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03017157
Subclinical Hypothyroidism and Acute Anterior Myocardial Infarction: Is it Cardio-protective or Not?
January 9, 2017 updated by: Hillel Yaffe Medical Center
The study plans to investigate whether recovery of the heart function after acute anterior myocardial infarction is dependent upon improvement in thyroid gland functioning.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Rami Abo Fane, MD, PhD
- Email: ramia@hy.health.gov.il
Study Locations
-
-
-
Hadera, Israel, 38100
- Hillel Yaffe Medical Center
-
Contact:
- Rami Abo Fane, MD, PhD
- Email: ramia@hy.health.gov.il
-
Principal Investigator:
- Rami Abo Fane, MD, PhD
-
-
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
Probability Sample
Study Population
Patients who have suffered anterior myocardial infarction who have been hospitalized in our hospital's cardiac unit.
Description
Inclusion Criteria:
- Have suffered anterior myocardial infarction
Exclusion Criteria:
- Do not receive thyroid treatment
- No history of ischemic heart disease
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 |
---|---|
Anterior Myocardial Infarction
Patients who have suffered anterior myocardial infarction in our hospital
|
Patients will undergo echo-cardiogram to determine improvement in their heart function and this will be compared to thyroid function
Blood test to determine thyroid function
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ejection Fraction Improvement
Time Frame: 40 days
|
Improvement in ejection fraction as shown in echo-cardiogram
|
40 days
|
Improvement in thyroid function
Time Frame: 40 days
|
Thyroid stimulating hormone (TSH) level will be normal.
|
40 days
|
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
January 1, 2017
Primary Completion (Anticipated)
April 1, 2017
Study Completion (Anticipated)
April 1, 2017
Study Registration Dates
First Submitted
December 21, 2016
First Submitted That Met QC Criteria
January 9, 2017
First Posted (Estimate)
January 11, 2017
Study Record Updates
Last Update Posted (Estimate)
January 11, 2017
Last Update Submitted That Met QC Criteria
January 9, 2017
Last Verified
January 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0096-16-HYMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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