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Truncal Blocks Versus Wound Infiltration for SICD

NCT04974762 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2022-08-04

No results posted yet for this study

Summary

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.

Conditions

  • Intraoperative Pain
  • Postoperative Pain

Interventions

PROCEDURE

Wound infiltration

Surgical wound infiltration by proceduralist

PROCEDURE

Truncal blocks

Truncal blocks provided by anesthesiology team for device placement

Sponsors & Collaborators

Principal Investigators

  • Ali Shariat, MD · Icahn School of Medicine at Mount Sinai

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-23
Primary Completion
2022-02-18
Completion
2022-02-18

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04974762 on ClinicalTrials.gov