Supraclavicular Versus Interscalene Block for Shoulder Surgery

NCT ID: NCT02486549

Last Updated: 2017-02-23

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

62 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-06-30

Study Completion Date

2017-02-28

Brief Summary

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The purpose of this study is to compare the supraclavicular block to interscalene block in patients undergoing arthroscopic shoulder surgery.

Detailed Description

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The aim of this study is to evaluate the efficacy of the supraclavicular block in comparison with interscalene block on postoperative pain, quality of recovery and side effects in patients undergoing arthroscopic shoulder surgery under general anesthesia.

Conditions

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Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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Supraclavicular Block

Ultrasound guided supraclavicular block with 20 ml of 0.25% bupivacaine will be performed

Group Type EXPERIMENTAL

Supraclavicular Block

Intervention Type PROCEDURE

Under ultrasound guidance an insulated needle is advanced with in- plane technique into the brachial plexus sheath and 20ml 0.25% bupivacaine will be administered

Bupivacaine

Intervention Type DRUG

20ml 0.25% bupivacaine will be injected for brachial plexus block

Ultrasound

Intervention Type DEVICE

The Ultrasound will be used for brachial plexus visualization

Interscalene block

Ultrasound guided inter scalene block with 20ml of 0.25% bupivacaine will be performed.

Group Type ACTIVE_COMPARATOR

Interscalene Block

Intervention Type PROCEDURE

Under ultrasound guidance an insulated needle will be placed through the middle scalene muscle,into the interscalene groove with in-plane technique and 20ml 0.25%bupivacaine will be administered into the brachial plexus

Bupivacaine

Intervention Type DRUG

20ml 0.25% bupivacaine will be injected for brachial plexus block

Ultrasound

Intervention Type DEVICE

The Ultrasound will be used for brachial plexus visualization

Interventions

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Supraclavicular Block

Under ultrasound guidance an insulated needle is advanced with in- plane technique into the brachial plexus sheath and 20ml 0.25% bupivacaine will be administered

Intervention Type PROCEDURE

Interscalene Block

Under ultrasound guidance an insulated needle will be placed through the middle scalene muscle,into the interscalene groove with in-plane technique and 20ml 0.25%bupivacaine will be administered into the brachial plexus

Intervention Type PROCEDURE

Bupivacaine

20ml 0.25% bupivacaine will be injected for brachial plexus block

Intervention Type DRUG

Ultrasound

The Ultrasound will be used for brachial plexus visualization

Intervention Type DEVICE

Other Intervention Names

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Marcaine

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing shoulder surgery in American Society of Anesthesiologists physical status I-II

Exclusion Criteria

* with a known allergy to study medications,
* chronic opioid use,
* ipsilateral upper limb neurological deficits,
* severe respiratory disease,
* coagulopathy
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tokat Gaziosmanpasa University

OTHER

Sponsor Role lead

Responsible Party

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Tuğba Karaman

Assistant Professor, M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tugba Karamanaraman, M.D.

Role: PRINCIPAL_INVESTIGATOR

Gaziosmanpasa University Medical School

Locations

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Gaziosmanpasa University Medical School

Tokat Province, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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artroscopy

Identifier Type: -

Identifier Source: org_study_id

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