Rectus Sheath Block in Cardiac Surgery
Recruiting
N/A
Interventional Study
Cardiac Disease
Postoperative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 85
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 75 (estimated)
- Sponsor
- Icahn School of Medicine at Mount Sinai · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* In order to be eligible to participate in this study, an individual must meet all of the following criteria:
1. Adults 18-85 years old
2. Scheduled to undergo cardiac procedures involving chest tubes
3. Male or female
Exclusion Criteria:
* An individual who meets any …
Contacts