Truncal Blocks Versus Wound Infiltration for SICD

Completed · Not applicable

Conditions studied: Intraoperative Pain, Postoperative Pain

In brief

This is a single-center, randomized and prospective trial of all patients undergoing S-ICD implantation. Subjects will only be eligible for this study if they are ≥ 18 years of age and eligible to undergo S-ICD implant at Mount Sinai Morningside Hospital. They will be randomized to receive either surgical infiltration of local anesthetic or truncal blocks. Intraoperative and postoperative data will be collected including total opioid use, pain scores postprocedure, total postoperative narcotic need and length of stay.

Key facts

Study ID

NCT04974762

Run by

Icahn School of Medicine at Mount Sinai

People needed

24

Starts

2019-01-23

Expected to finish

2022-02-18

Last updated by the study team

2022-08-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients over 18 years of age
• Patients undergoing S-ICD placement

You may not qualify if…

• Allergy to amide local anesthetics

Where it is running

• Mount Sinai Morningside Hospital Center — New York, New York, United States

Full record on ClinicalTrials.gov

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