Pectoral Nerve Blocks (PECs) for Cardiovascular Implantable Electronic Device Placement

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Pain, Postoperative, Pain, Acute, Pain, Chest, Pain, Satisfaction, Patient, Opioid Use, Unspecified, Opioids; Harmful Use

In brief

The purpose of this study is to determine whether administration of a pectoral nerve blocks (Pecs I and II) with 0.25% bupivacaine are more effective as compared to placebo to provide analgesia for cardiac implantable electronic device (CIED) placement in cardiac electrophysiology lab

Key facts

Study ID
NCT05283980
Run by
Beth Israel Deaconess Medical Center
People needed
62
Starts
2022-11-17
Expected to finish
2024-03-29
Last updated by the study team
2026-07-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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