NCT03269838

Brief Summary

To correlate QT dispersion on 12-lead surface ECG with myocardial reperfusion evaluated by myocardial blush grade and Thrombolysis in myocardial infarction (TIMI) flow grades in patients with ST elevation myocardial infarction treated by Primary Per cutaneous coronary intervention

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
235

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2018

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

August 27, 2017

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 1, 2017

Completed
10 months until next milestone

Study Start

First participant enrolled

July 1, 2018

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2019

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2019

Completed
Last Updated

July 3, 2018

Status Verified

June 1, 2018

Enrollment Period

1 year

First QC Date

August 27, 2017

Last Update Submit

June 30, 2018

Conditions

Outcome Measures

Primary Outcomes (2)

  • Correlation of QT dispersion on 12-lead surface ECG with myocardial reperfusion

    Use 12 lead ECG to calculate QT interval and QT dispersion comparing ECG before and after myocardial reperfusion.

    1 year

  • Evaluation of myocardial perfusion by coronary angiography by assessing 2 parameters TIMI flow and myocardial blush grade

    Use coronary angiography to detect myocardial blush grade and TIMI flow to assess myocardial reperfusion

    1 year

Interventions

ECGDIAGNOSTIC_TEST

Primary Percutaneous coronary intervention

Also known as: Primary Percutaneous coronary intervention

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

This cross sectional observational study will include patients with acute STEMI of different ages from cardiology department, Assiut University Hospital who will undergo primary percutaneous coronary intervention (PCI).

You may qualify if:

  • Patients will be enrolled in this study if they fulfilled the criteria of acute ST elevation myocardial infarction eligible to be treated with primary Percutaneous coronary intervention

You may not qualify if:

  • Non-ST elevation myocardial infarction, prior history of myocardial infarction or surgical revascularization,
  • Electrolyte disturbance.
  • history of medications that may affect QT (anti-arrhythmic, anti-psychotic, and anti-depressant drugs),
  • patients with cardiogenic shock or needing IABP.
  • patients with previous CABG.
  • Patients with implantable devices and pacemakers.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Assiut university

Asyut, 71641, Egypt

RECRUITING

Related Publications (1)

  • Karahan Z, Yaylak B, Ugurlu M, Kaya I, Ucaman B, Ozturk O. QRS duration: a novel marker of microvascular reperfusion as assessed by myocardial blush grade in ST elevation myocardial infarction patients undergoing a primary percutaneous intervention. Coron Artery Dis. 2015 Nov;26(7):583-6. doi: 10.1097/MCA.0000000000000285.

    PMID: 26166018BACKGROUND

MeSH Terms

Conditions

ST Elevation Myocardial Infarction

Interventions

Electrocardiography

Condition Hierarchy (Ancestors)

Myocardial InfarctionMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Intervention Hierarchy (Ancestors)

Heart Function TestsDiagnostic Techniques, CardiovascularDiagnostic Techniques and ProceduresDiagnosisElectrodiagnosis

Study Officials

  • Hatem Helmy

    assistant professor

    STUDY CHAIR
  • Hosam Hasan

    professor

    STUDY CHAIR

Central Study Contacts

Marina Samir, master

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 27, 2017

First Posted

September 1, 2017

Study Start

July 1, 2018

Primary Completion

July 1, 2019

Study Completion

September 1, 2019

Last Updated

July 3, 2018

Record last verified: 2018-06

Locations