Cardiac Implantable Electronic Device Implantation With and Without Pectoral Nerve Block

NCT ID: NCT03061292

Last Updated: 2020-10-08

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-25

Study Completion Date

2020-11-30

Brief Summary

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Implantation of cardiac implantable electronic devices are generally carried out using intermittent intravenous conscious sedation combined with local anaesthesia. The main advantage of this technique is in avoiding the potential risks of general anaesthesia. However, the use of this Sedation - Local Anaesthesia technique is not without complications. Peri -procedural hypoxaemia and hypotension are well recognised complications of this technique.

The pectoral nerves (Pecs) blocks are novel techniques to block the pectoral, intercostobrachial, third to sixth intercostals, and the long thoracic nerves. PECS block targets the lateral and median pectoral nerves at an interfascial plane between the pectoralis major and minor muscles.

A case report by Fujiwara et al has described the use of this technique to provide good analgesia during and after these implantation procedures surgery. Pectoral nerves block along with minimal sedation has been used as a safe technique in our local set up as well.

Hence, we propose a randomized, single center, controlled trial on patients undergoing cardiac implantable electronic device implantation with local anaesthesia and sedation with and without Pectoral Nerve Block.

Detailed Description

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Intervention group:

Pectoral nerve block will be performed by anaesthetist (not blinded) in cardiac catheterization laboratory using ultrasound guidance and strict aseptic technique.

Control group:

A sham "block" will be performed by anaesthetist in cardiac catheterization laboratory using strict aseptic technique.

Patients of both groups will be monitored by the Cardiologist ( performing the procedure) and the Nurse from the monitoring room.

A minimum period of 15 minutes will be allowed following the block, prior to device implantation procedure by cardiologist.

Numeric rating scale (NRS) will be used for assessment of pain. The assessment will be carried out at every 15 minutes from the start of the procedure till the end of the procedure (0, 15, 30, 45, 60 minutes etc) and also at specific time points. Numerical rating scale will also be assessed when the patient experiences pain at any point and in the recovery room (0, 15, 30 and if needed, 45, 60 minutes).

Further post-operative pain scores will be collected at 4 hours and 8 hours post-procedure.

Conditions

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Cardiac IED Implantation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Study Groups

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Pectoral Nerve Block

Patients undergoing cardiac implantable electronic device implantation with local anaesthesia and sedation with pectoral nerve block

Group Type EXPERIMENTAL

Pectoral Nerve Block

Intervention Type PROCEDURE

Without Pectoral Nerve Block

Patients undergoing cardiac implantable electronic device implantation with local anaesthesia and sedation without pectoral nerve block

Group Type SHAM_COMPARATOR

Without Pectoral Nerve Block

Intervention Type PROCEDURE

Interventions

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Pectoral Nerve Block

Intervention Type PROCEDURE

Without Pectoral Nerve Block

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Fulfilled the indication for CIED implantation as defined in 2008 guidelines for device-based therapy of cardiac rhythm abnormalities

Exclusion Criteria

* Pregnant
* Those who receives subcutaneous implantable cardioverter defibrillator
* Vulnerable subjects (children, prisoners, cognitive impaired persons)
* Known history of allergy to local anaesthetic medications
Minimum Eligible Age

21 Years

Maximum Eligible Age

95 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Changi General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Changi General Hospital

Singapore, , Singapore

Site Status RECRUITING

Countries

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Singapore

Central Contacts

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Vern Hsen Tan, MBBS

Role: CONTACT

Facility Contacts

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CTRU

Role: primary

67888833

Other Identifiers

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PECS

Identifier Type: -

Identifier Source: org_study_id

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