Cardiac Implantable Electronic Device Implantation With and Without Pectoral Nerve Block
NCT ID: NCT03061292
Last Updated: 2020-10-08
Study Results
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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UNKNOWN
NA
120 participants
INTERVENTIONAL
2016-07-25
2020-11-30
Brief Summary
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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.
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Detailed Description
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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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Study Design
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RANDOMIZED
PARALLEL
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
Pectoral Nerve Block
Without Pectoral Nerve Block
Patients undergoing cardiac implantable electronic device implantation with local anaesthesia and sedation without pectoral nerve block
Without Pectoral Nerve Block
Interventions
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Pectoral Nerve Block
Without Pectoral Nerve Block
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Those who receives subcutaneous implantable cardioverter defibrillator
* Vulnerable subjects (children, prisoners, cognitive impaired persons)
* Known history of allergy to local anaesthetic medications
21 Years
95 Years
ALL
No
Sponsors
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Changi General Hospital
OTHER
Responsible Party
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Locations
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Changi General Hospital
Singapore, , Singapore
Countries
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Central Contacts
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Facility Contacts
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CTRU
Role: primary
Other Identifiers
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PECS
Identifier Type: -
Identifier Source: org_study_id
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