Extensively Diseased Left Anterior Descending Coronary Artery: On Pump vs Off Pump CABG?

CAD - Coronary Artery Disease Clinical Trial

Official title:

Extensively Diseased Left Anterior Descending Coronary Artery: On Pump vs Off Pump CABG?

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05442723
• Other study ID #: AssiutMed
• Status: Recruiting
• Phase: N/A
• Start date: February 25, 2022
• Est. completion date: March 1, 2023

Study information

• Verified date: June 2022
• Source: Assiut University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Diseased left Anterior descending coronary artery (LAD) is one of the most challenging conditions in Bypass surgery. we investigate whether on-pump coronary artery bypass grafting (CABG) is more beneficial in those critical patients or off-pump surgery.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: March 1, 2023
• Est. primary completion date: February 24, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 30 Years and older

Eligibility

Inclusion Criteria:

• any patient with diffuse LAD disease indicated for open heart surgery

Exclusion Criteria:

• no concomitant valve disease

• any patient can be treated by medical treatment or PCI

Related Conditions & MeSH terms

• CAD - Coronary Artery Disease
• Coronary Artery Disease
• Coronary Disease

Intervention

Procedure:
• On-Pump CABG
coronary artery grafting by using cardiopulmonary bypass machine
• Off-Pump CABG
coronary artery grafting by beating heart technique

Locations

Country	Name	City	State
Egypt	Assiut university heart hospital	Assiut

Sponsors (1)

Lead Sponsor	Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	mortality	follow up post-operative track of the patient for any noticed mortality rate	30 days post operative
Primary	Morbidity	follow up post-operative track of the patient for any noticed complications	60 days post operative