Expression of microRNA-133a and microRNA-208b in Acute Myocardial Infarction
NCT ID: NCT05692752
Last Updated: 2023-01-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
10 participants
OBSERVATIONAL
2022-12-28
2023-01-14
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of Plasma Non-coding RNAs as Biomarkers in Coronary Heart Disease
NCT02751060
The Use of Blood Biochemical Markers for Diagnostics of Heart Muscle Diseases
NCT05726695
Genetics of Ischemic Cardiomyopathy
NCT05508269
Circulating microRNAs and Adverse Cardiovascular Outcomes in Patients With Coronary Artery Disease
NCT03635255
Potential Diagnostic and Prognostic Value of microRNAs for the Patients of Acute Coronary Syndrome
NCT02755207
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Identify new diagnostic biomarkers based on miRNAs, researchers examine the expression of miR-133a and 208b at various time points (04 hours, 08 hours, 12 hours, 24 hours, 48 hours) following the development of the infarct and compared it to the traditional myocardial infarction biomarkers cTnl and CK-MB.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Test Group
The study group included 10 patients,
1. men and women
2. between age of 35-60 year
3. chest pain lasting for at least 30 minutes,
4. electrocardiogram (ECG) finding that display ST-segment elevation (STEMI)
No intervention
Expression of miR-133a \&208b at 4, 8, 12, 24 and 48 hours from the first appearance of myocardial infarction (MI) symptoms
Control Group
The study group included 10 patients,
1. men and women
2. between age of 35-60 year
3. having no complaint of health issue,
No intervention
Expression of miR-133a \&208b at 4, 8, 12, 24 and 48 hours from the first appearance of myocardial infarction (MI) symptoms
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
No intervention
Expression of miR-133a \&208b at 4, 8, 12, 24 and 48 hours from the first appearance of myocardial infarction (MI) symptoms
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Acute episode of Myocardial Infarction
3. With No history of previous Myocardial Infarction Treatment
Exclusion Criteria
2. Previously Known patients of Myocardial infacrtion
3. Previous medication
35 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
German University in Cairo
OTHER
Islamia University of Bahawalpur
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hafiz Abdul Sattar Hashmi
Lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sally I Hassanien, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Biochemistry Department German University in Cairo, 11835, Cairo, Egypt
Hafiz A Sattar, M.Phil
Role: PRINCIPAL_INVESTIGATOR
University College of Conventional Medicine, The Islamia University of Bahawalpur, Punjab, Pakistan
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Biochemistry Department, Faculty of Pharmacy and Biotechnology, German University in Cairo, Main Entrance Al Tagamoa Al Khames
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
UCCM/2022/EGT/01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.