PECs for Implantable Cardiac Electronic Device Insertion

NCT ID: NCT05528627

Last Updated: 2022-09-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-01

Study Completion Date

2021-10-15

Brief Summary

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The aim of this study is to evaluate the feasibility of the Pectoralis Nerve (PECS) block for CIED insertion.

Detailed Description

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Implantable Cardiac Electronic Device (CIED) insertion can be performed under local anesthesia, regional anesthesia, or general anesthesia. Novel regional blocks may improve pain management for such patients and can shorten their length of stay in the hospital. At the study, the investigators aimd to evaluate the efficacy and feasibility of the PECS block for CIED insertion procedure.

Conditions

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Cardiac Implantable Electronic Device Nerve Block Anesthesia Analgesia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Pectoral Nerve (PECS) block

Pectoral Nerve (PECs) block was performed at the surgical side 30 min before the procedure

Group Type OTHER

Pectoral Nerve (PECs) block

Intervention Type OTHER

Pectoral Nerve (PECS) blocks were performed on the side of surgery, using the ultrasound-guided technique 30 min before the implantable cardiac electronic device (pacemaker, implantable cardioverter defibrillator) insertion procedure

Interventions

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Pectoral Nerve (PECs) block

Pectoral Nerve (PECS) blocks were performed on the side of surgery, using the ultrasound-guided technique 30 min before the implantable cardiac electronic device (pacemaker, implantable cardioverter defibrillator) insertion procedure

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* American Society of Anaesthesiologists grade II-IV patients
* in the age group of 18-80 years,
* Patients undergoing CIED insertion

Exclusion Criteria

* pre-existing infection at the block site,
* coagulopathy,
* morbid obesity (Body mass index \>35 kg m-2 ),
* allergy to local anaesthetics,
* decreased pulmonary reserve,
* psychiatric illness
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Antalya Training and Research Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mustafa Kilin, M.D.

Role: PRINCIPAL_INVESTIGATOR

Antalya Training and Research Hospital

Locations

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Antalya Training and Research Hospital

Antalya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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mustafa1

Identifier Type: -

Identifier Source: org_study_id

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