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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05686395
Other study ID # IRB0010038
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date January 2024

Study information

Verified date January 2023
Source Tanta University
Contact HOSAMELDIN ELDIB, MASTER
Phone 00201000504087
Email dr.semsem337@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will be conducted to compare the perioperative analgesic efficacy of ultrasound - guided interscalene brachial plexus block versus combined shoulder anterior capsular block and anterior suprascapular nerve block for arthroscopic shoulder surgeries.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date January 2024
Est. primary completion date August 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria: - Patients aged 20-65 years of both sexes, with American Society of Anesthesiologists (ASA) physical status I or II admitted for arthroscopic shoulder surgery. Exclusion Criteria: - Patient refusal. - Uncooperative patient. - Patient with neurological deficit. - Patients with respiratory disorders. - Patient with bleeding disorders. - Infection at the block injection site. - Patients with history of allergy to local anesthetics.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ultrasound-guided Interscalene Block group
ultrasound guided interscalene block versus combined ultrasound guided shoulder anterior capsular block and suprascapular nerve block for arthroscopic shoulder surgery
Combined Ultrasound guided shoulder anterior capsular block and suprascapular nerve block
Combined Ultrasound guided shoulder anterior capsular block and suprascapular nerve block
Drug:
Bupivacaine
bupivacaine 0.25%.

Locations

Country Name City State
Egypt Faculty of Medicine Tanta University Tanta

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary post operative analgesic consumption The first 24 hours post operative analgesic consumption 24 hours after surgery
Secondary Visual Analogue score (VAS) in the first 24 hours after surgery - Postoperative pain intensity will be assessed in the first 24 hour using VAS score where (0 = no pain and 100 = the worst imaginable pain) first 24 hours after surgery
Secondary Patient satisfaction score Patient satisfaction score will be assessed on the basis of a questionnaire and graded on a 4-point scale (excellent/good/fair/poor). first 24 hours after surgery
Secondary The incidence of hemi diaphragmatic paralysis hemidiaphragmatic paralysis after block immediately before block and immediately after procedure
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