RecruitingNot ApplicableNCT05833048

Rectus Sheath Block in Cardiac Surgery


Sponsor

Icahn School of Medicine at Mount Sinai

Enrollment

75 participants

Start Date

Jul 29, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective, randomized study. The purpose of this study is to evaluate the effect of post-surgical pain control of a type of peripheral nerve block, Rectus Sheath Block. 1. Does the rectus sheath block decrease opioid consumption postoperatively after cardiac surgery? 2. Does the rectus sheath block decrease VAS pain scores postoperatively after cardiac surgery? Study participants will be assigned to receive either rectus sheath block or no block.


Eligibility

Min Age: 18 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Rectus sheath block for people with cardiac disease and postoperative pain. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURERectus sheath block

Participants will receive an ultrasound guided rectus sheath block with local anesthetic


Locations(1)

Mount Sinai Morningside Hospital Center

New York, New York, United States

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NCT05833048


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