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Parasternal blocks for Coronary Artery Bypass Surgery

Phase 3
Waitlist Available
Research Sponsored by Jewish General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately as intervention is performed
Awards & highlights

Study Summary

This trial will test how well parasternal blocks with local anesthetic drugs work to relieve pain after CABG surgery.

Who is the study for?
This trial is for patients scheduled for elective or urgent coronary artery bypass surgery who can give consent. It's not suitable for those with regular opioid use or chronic pain history.Check my eligibility
What is being tested?
The study tests the effectiveness of parasternal blocks, a type of regional anesthesia, in managing post-surgery pain compared to standard care after coronary artery bypass grafting.See study design
What are the potential side effects?
Parasternal blocks may cause side effects like localized discomfort, potential nerve damage, infection at the injection site, and inadequate pain relief requiring additional analgesics.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from icu arrival until first ambulation (approximately first 72 hours postoperatively)
This trial's timeline: 3 weeks for screening, Varies for treatment, and from icu arrival until first ambulation (approximately first 72 hours postoperatively) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Pain with inspirometry at 24 hours after surgery
Secondary outcome measures
Ambulation
Amount of rescue analgesia administered
Hospital Length of Stay
+7 more
Other outcome measures
Incidence of a pneumothorax
Incidence of bradycardia
Incidence of hyperglycemia
+6 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Intervention groupExperimental Treatment1 Intervention
Patients will receive bilateral parasternal blocks at the end of cardiac surgery.
Group II: Control groupPlacebo Group1 Intervention
Patients will receive all standard care as per the hospital protocols.

Find a Location

Who is running the clinical trial?

Jewish General HospitalLead Sponsor
137 Previous Clinical Trials
271,984 Total Patients Enrolled

Media Library

Parasternal blocks Clinical Trial Eligibility Overview. Trial Name: NCT05191745 — Phase 3
Coronary Artery Bypass Surgery Research Study Groups: Intervention group, Control group
Coronary Artery Bypass Surgery Clinical Trial 2023: Parasternal blocks Highlights & Side Effects. Trial Name: NCT05191745 — Phase 3
Parasternal blocks 2023 Treatment Timeline for Medical Study. Trial Name: NCT05191745 — Phase 3

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many guinea pigs are currently testing this new drug?

"The information available on clinicaltrials.gov verifies that this study is currently looking for patients to enroll. The trial was originally posted on January 26th, 2022 and updated most recently on July 27th, 2022. 1 site is recruiting a total of 60 participants."

Answered by AI

Are we still looking for patients to participate in this experiment?

"Yes, this study is currently enrolling patients. Information on clinicaltrials.gov reveals that the trial was first posted on January 26th, 2022 and last updated on July 27th, 2022."

Answered by AI

Is there a potential for long-term harm with Parasternal blocks?

"Given that this is a Phase 3 trial with efficacy data and multiple rounds of safety data, our team at Power gives Parasternal blocks a score of 3 for safety."

Answered by AI
~19 spots leftby Apr 2025