ESP/PIF for Sternotomy

Status Recruiting

Clinical Trial Summary

This is a randomized study. The purpose of this study is to evaluate the effect of post-surgical pain control of two types of peripheral nerve blocks, specifically erector spinal plane (ESP) block and pecto-intercostal fascial (PIF) plane block. 90 subjects, from 18-85 years of age, undergoing cardiac surgery with median sternal incision will be enrolled at Mount Sinai Morningside Hospital Center. Study participation will last from the time of pre-operative evaluation to 72 hours after surgery. Subjects will be randomly assigned to receive 1 of the 3 different regimens at the beginning of surgery. Opioid consumption and pain scores after surgery will be evaluated. Though unlikely, risks include systemic absorption of local anesthetic, which can result in both central nervous system and cardiac toxicity.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04985500
Study type	Interventional
Source	Icahn School of Medicine at Mount Sinai
Contact	Shenghao Fang, M.D.
Phone	434-326-8499
Email	shenghao.fang@mountsinai.org
Status	Recruiting
Phase	Early Phase 1
Start date	July 8, 2021
Completion date	August 2024

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