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ACTIVE NOT RECRUITING
NCT04985500
EARLY_PHASE1

ESP/PIF for Sternotomy

Sponsor: Icahn School of Medicine at Mount Sinai

View on ClinicalTrials.gov

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.

Official title: Erector Spinae Plane Block vs. Pecto-intercostal Fascial Plane Block vs. Control for Sternotomy: A Prospective Randomized Trial

Key Details

Gender

All

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

225

Start Date

2021-07-09

Completion Date

2025-12-31

Last Updated

2025-07-15

Healthy Volunteers

No

Interventions

PROCEDURE

ESP block

peripheral nerve block

PROCEDURE

PIF block

peripheral nerve block

PROCEDURE

Ultrasound

Ultrasound guidance

DRUG

Bupivacain

10-20 mL of 0.25% bupivacaine

Locations (1)

Mount Sinai Morningside Hospital

New York, New York, United States