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Study identifier: NCT05833048 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Rectus Sheath Block in Cardiac Surgery

Condition: Cardiac Disease · Postoperative Pain  ·  Sponsor: Icahn School of Medicine at Mount Sinai

PhaseNA
Planned participants75
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Ali Shariat, MD  ·  212-523-2500  ·  AliNima.Shariat@mountsinai.org

Himani Bhatt, DO  ·  212-523-2500  ·  himani.bhatt@mountsinai.org

Always discuss trial participation with your own doctor first.

Locations (1)

Mount Sinai Morningside Hospital CenterNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05833048