Rectus Sheath Block in Cardiac Surgery

Part of paid clinical trials in New York, New York.

Sponsor
Icahn School of Medicine at Mount Sinai
Study ID
NCT05833048
Status
Recruiting
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Conditions

  • Cardiac Disease
  • Postoperative Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 85 Years
Healthy Volunteers
Not accepted

Interventions

  • Rectus sheath block — PROCEDURE
    Participants will receive an ultrasound guided rectus sheath block with local anesthetic

Study Details

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.

Key Dates

Start date
Jul 29, 2024
Status verified
Sep 2025
Primary completion
Mar 30, 2026
Completion
Sep 7, 2026

Study Design

Enrollment
75 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Rectus Sheath Block
  • No Intervention: No block

Primary Outcome Measure

Opioid consumption [ Time Frame: 72 hours postoperatively ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Mount Sinai Morningside Hospital CenterNew YorkNew York10023
Ali Shariat, MD
[email protected]
212-523-2500

Find similar trials in New York, NY

By research site
Mount Sinai Morningside Hospital Center· New York, NY

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