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Ultrasound-Guided Extrafascial Versus Intrafascial Interscalene Brachial Plexus Block in Shoulder Arthroscopy

T

Tanta University

Status

Unknown

Conditions

Arthroscopy
Intrafascial Interscalene Brachial Plexus Block
Analgesia

Treatments

Drug: Bupivacaine
Procedure: Intrafascial interscalene brachial plexus block
Procedure: Extrafascial interscalene brachial plexus block group

Study type

Interventional

Funder types

Other

Identifiers

NCT05222334
33802/4/20

Details and patient eligibility

About

The aim of the study is to compare the diaphragmatic excursion and postoperative analgesia in the extrafascial versus intrafascial Interscalene brachial plexus block in patients undergoing shoulder arthroscopy.

Enrollment

50 estimated patients

Sex

All

Ages

21 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients of both sexes aged (21-60years) with American Society of Anesthesiologists (ASA) physical status I/II scheduled for shoulder arthroscopy

Exclusion criteria

  1. Patient refusal.
  2. Pre-existing (obstructive or restrictive) pulmonary disease.
  3. Bleeding disorders (coagulopathy).
  4. Mental dysfunction.
  5. History of allergy to local anesthetics.
  6. Pregnancy
  7. Body mass index (BMI) >40

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Intrafascial interscalene brachial plexus block group
Experimental group
Description:
The patients will receive 10 ml of 0.5% bupivacaine for intrafascial interscalene brachial plexus block group
Treatment:
Drug: Bupivacaine
Procedure: Intrafascial interscalene brachial plexus block
Extrafascial interscalene brachial plexus block group
Experimental group
Description:
The patients will receive 10 ml of 0.5% bupivacaine for extrafascial interscalene brachial plexus block group
Treatment:
Drug: Bupivacaine
Procedure: Extrafascial interscalene brachial plexus block group

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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