NCT06893601View on ClinicalTrials.gov

The Effect of Parasternal Block on Postoperative Pain in Patients Undergoing Coronary Artery Bypass Graft Surgery

PHASE2CompletedINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

January 18, 2020

Primary Completion Date

October 17, 2020

Study Completion Date

October 17, 2020

Conditions
Postoperative PainICU HospitalizationExtubation Time
Interventions
DRUG

Parasternal block

A block containing 0.9% NaCl solution was applied to the Saline group just before the sternum was closed by the surgeon, while a bilateral parasternal block using 0.25% bupivacaine was applied to the bupivacaine group. The solutions used for the parasternal block were colorless and indistinguishable to ensure blinding.

Trial Locations (1)

Unknown

Aydin Adnan Menderes University, Aydin

All Listed Sponsors
lead

Aydin Adnan Menderes University

OTHER

NCT06893601 - The Effect of Parasternal Block on Postoperative Pain in Patients Undergoing Coronary Artery Bypass Graft Surgery | Biotech Hunter | Biotech Hunter