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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06424028
Other study ID # IRB-62/2023
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 20, 2024
Est. completion date August 19, 2024

Study information

Verified date May 2024
Source National Institute of Cardiovascular Diseases, Pakistan
Contact Rajesh Kumar, MBBS, FCPS
Phone +923337306090
Email rajeshnarsoolal@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This Study aims to provide an assessment of clinical presentation, management, hospital course, and prognosis of acute right ventricular infarction presenting with or without Inferior or infero-posterior wall Myocardial Infarction and the assessment of composite adverse clinical outcome after reperfusion in-hospital and post-discharge (in 30 Days Prognosis).


Description:

After fulfilling the eligibility criteria, informed consent will be obtained from all the patients regarding using data for research while maintaining anonymity.Data will be collected for various patient, system, and procedure related characteristics with the help of a predefined structured proforma consisted of demographic data, clinical presentation, history and co-morbid conditions, and angiographic and procedural characteristics. All the recruited patients will be kept under observiton during the hospital stay and a telephonic follow-up will be carried out after 30-days of discharge and occurrence of the MACE will be recorded. Univariate and multivariable binary logistic regression analysis will be performed to determine the clinical predictors of RVI. Odds ratio (OR) along with 95% confidence interval (CI) will be reported. The statistical significance criteria will be set as p-value<0.05. For data verification, 10% of the data will be cross-checked with the source document (Patient file).


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date August 19, 2024
Est. primary completion date July 19, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients of Inferior, infero-lateral and infero-posterior wall MI with and without RV infarction undergoing PPCI. - Both male and female patients. - Patients of age = 18 years. Exclusion Criteria: • Patients who will not give consent for participation.

Study Design


Intervention

Other:
Right Ventricular Infarct
Consecutive patients presented with isolated inferior, infero-posterior and inferolateral wall MI with or without acute right ventricular infarction.

Locations

Country Name City State
Pakistan National Institute of Cardiovascular Diseases Karachi Sindh

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Cardiovascular Diseases, Pakistan

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Composite adverse clinical outcome Atleast one adverse event, such as pump failure, cerebrovascular accident (CVA), stent thrombosis, major bleeding, contrast-induced nephropathy (CIN), ventricular arrhythmias, or mortality. Upto 30 days from admission
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