NCT03308539

Brief Summary

is to test the hypotheses that epicardial adipose tissue can be a marker of severity of coronary artery disease in myocardial infarction patients

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 6, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 12, 2017

Completed
20 days until next milestone

Study Start

First participant enrolled

November 1, 2017

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2017

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2018

Completed
Last Updated

October 12, 2017

Status Verified

October 1, 2017

Enrollment Period

1 month

First QC Date

October 6, 2017

Last Update Submit

October 11, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • measurement of epicardial adipose tissue as marker of severity of coronary artery disease in myocardial infarction patients.

    epicardial adipose tissue measurement using transthoracic echocardiography and cardiac magnetic resonance

    one year

Study Arms (1)

myocardial infarction patients

transthoracic echocardiography and cardiac magnetic resonance

Radiation: echocardiography and cardiac magnetic resonance

Interventions

transthoracic echocardiography and magnetic resonance imaging of the heart

myocardial infarction patients

Eligibility Criteria

AgeUp to 90 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

acute myocardial infarction patiens not previously underwent percutaneous coronary angiography or coronary artery bypass grafting

You may qualify if:

  • Normal thoracic shape
  • Sinus rhythm
  • without severe respiratory diseases

You may not qualify if:

  • contraindication for cardiac magnetic resonance.
  • Patients who previously underwent coronary artery bypass grafting or percutaneous coronary angiography prior to admission
  • history of chronic kidney disease with glomerular filtration rate \<30 mL/min
  • pericardial and/or pleural effusion.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Jacqueline George

Asyut, Single, Egypt

RECRUITING

Related Publications (1)

  • Desferrioxamine and transfusional iron overload. Lancet. 1978 Mar 4;1(8062):479-80. No abstract available.

MeSH Terms

Conditions

Myocardial Infarction

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Central Study Contacts

jacqueline george, master

CONTACT

hosam hassan el araby, pofessor

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

October 6, 2017

First Posted

October 12, 2017

Study Start

November 1, 2017

Primary Completion

December 1, 2017

Study Completion

September 1, 2018

Last Updated

October 12, 2017

Record last verified: 2017-10

Locations