RECRUITING

Rectus Sheath Block in Cardiac Surgery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Rectus Sheath Block in Cardiac Surgery

Quick Facts

Study Start:2024-07-29
Study Completion:2025-08-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05833048

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * In order to be eligible to participate in this study, an individual must meet all of the following criteria:
  2. 1. Adults 18-85 years old
  3. 2. Scheduled to undergo cardiac procedures involving chest tubes
  4. 3. Male or female
  1. * An individual who meets any of the following criteria will be excluded from participation in this study:
  2. 1. ASA class V
  3. 2. Urgent or emergent surgery
  4. 3. Contraindications to administration of local anesthesia (e.g. local anesthetic allergy)
  5. 4. History of substance abuse or chronic opioid use
  6. 5. Patient refusal or inability to consent

Contacts and Locations

Study Contact

Ali Shariat, MD
CONTACT
212-523-2500
AliNima.Shariat@mountsinai.org
Himani Bhatt, DO
CONTACT
212-523-2500
himani.bhatt@mountsinai.org

Study Locations (Sites)

Mount Sinai Morningside Hospital Center
New York, New York, 10023
United States

Collaborators and Investigators

Sponsor: Icahn School of Medicine at Mount Sinai

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-29
Study Completion Date2025-08-30

Study Record Updates

Study Start Date2024-07-29
Study Completion Date2025-08-30

Terms related to this study

Keywords Provided by Researchers

  • cardiac surgery
  • regional anesthesia

Additional Relevant MeSH Terms

  • Cardiac Disease
  • Postoperative Pain