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NCT06457815 Clinical Trial

Iron Deficiency in Acute Myocardial Infarction: Prevalence Pilot Study

Acute Myocardial Infarction Clinical Trial

— IDAMI Pilot  

Official title:
Iron Deficiency in Acute Myocardial Infarction: Prevalence Pilot Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06457815
Other study ID # ACU020
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 29, 2024
Est. completion date August 30, 2024

Study information
Verified date June 2024
Source South Tees Hospitals NHS Foundation Trust
Contact David Austin, MD
Phone 01642850850
Email david.austin@nhs.net
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acute Myocardial Infarction (heart attacks) affect about 86000 people each year in the UK. Given this large number of people, it is important that health teams look at ways to ensure the best care to improve outcomes after a heart attack. In related heart conditions, the role of iron is important, but there isn't much information about what effect iron levels have on patients following a heart attack. We want to plan a large scale study to look at this, but need some early data to understand how many patients have low iron levels. This small study will take part at one NHS Trust and will test for iron levels in all patients who provide consent (we expect up to 70 patients will take part). We will also collect data from medical notes for these patients and use all of this information together to understand more about iron and to plan a larger study.

Recruitment information / eligibility
Status Recruiting
Enrollment 70
Est. completion date August 30, 2024
Est. primary completion date July 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion: 1. - Adults patients who sign an informed consent form. 2. - Type 1 myocardial infarction within the previous 10 days Exclusion 1 - Not fulfilling inclusion criteria

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United Kingdom South Tees Hospitals NHS Foundation Trust Middlesbrough Teesside
United Kingdom South Tees Hospitals NHS Foundation Trust Middlesbrough

Sponsors (1)
Lead Sponsor Collaborator
South Tees Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary Prevalence of iron deficiency Prevalence of iron deficiency in a population of patients following acute MI. within 10 days of acute MI
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