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NCT05191745

Long-acting Parasternal Blocks for Analgesia After Cardiac Surgery

Completed Phase 3 Last updated 10 June 2024
What this trial tests

Phase 3 trial testing Parasternal blocks in Coronary Artery Bypass Graft Surgery in 60 participants. Completed in 1 June 2024.

Timeline
26 January 2022
Primary endpoint
28 April 2023
1 June 2024

Quick facts

Lead sponsorJewish General Hospital
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment60
Start date26 January 2022
Primary completion28 April 2023
Estimated completion1 June 2024
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Jewish General Hospital

Who can join

18 and older, any sex, with Coronary Artery Bypass Graft Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a randomized, double-blind, controlled clinical trial is to evaluate the duration of efficacy of parasternal blocks with the use of local anesthetic adjuncts for analgesia after coronary artery bypass grafting surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Parasternal blocks

Trials testing the same drug.

Other recruiting trials for Coronary Artery Bypass Graft Surgery

Currently open trials in the same condition.

Other Jewish General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05191745.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing