Comparison of Interscalene Block and Suprascapular With Axillary Block

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

76 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-30

Study Completion Date

2022-01-31

Brief Summary

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In this study, the investigators are going to compare the analgesia effectiveness of interscalane block and suprascapular with axillary block in shoulder arthroplasties

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Detailed Description

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In the preoperative period, the participants will be taken to the block room. The participants will be monitored, standard sedation will be applied.

The first group will be get interscalene block. The second group will be get suprascapular and axillary block. The third group patient will be get no block. Afterwards, the participants will be operated under general anesthesia. A patient-controlled analgesia device will be attached to each group of participants and their postoperative follow-up will be made.

Conditions

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Shoulder Arthroplasty Ultrasound Guided

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Study group - Study group- Control group

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

open

Study Groups

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Study group: interscalene block + IV PCA

preop usg guided interscalene block and IV PCA

Group Type EXPERIMENTAL

interscalene block

Intervention Type PROCEDURE

peripheral nerve block

Study group: suprascapular block + axillary block + IV PCA

preop usg guided suprascapular block + axillary block and IV PCA

Group Type EXPERIMENTAL

suprascapular block + axillary block

Intervention Type PROCEDURE

peripheral nerve block

Control group: IV PCA

no block + IV PCA

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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interscalene block

peripheral nerve block

Intervention Type PROCEDURE

suprascapular block + axillary block

peripheral nerve block

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* accepting the study protocol,
* age older than 18 years and younger than 90 years,
* undergoing shoulder arthroplasty surgery
* the American Society of Anesthesiologist (ASA) physical status of I-II-III-IV

Exclusion Criteria

* severe respiratory distress
* patients with local anesthetic allergy
* contralateral hemidiaphragmatic parrhesia
* recurrent laryngeal nerve palsy
* infection at the injection site
* coagulation disorder

Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No