Ain shams university hospitals
Cairo, Egypt
NCT Number: NCT06609590
The patients will be randomized into 2 equal groups by a computer-generated random numbers table, named group A, B.
Group A: Patients will receive Anterior glenoid block combined with suprascapular nerve block.
Group B: Patients will receive conventional interscalene block.
In group A, the patient will be supine for anterior glenoid block.
The suprascapular nerve will be identified as it branch off from the superior trunk and will be traced until it courses beneath the inferior belly of the omohyoid muscle.
In group B, interscalene brachial plexus block will be performed.
The primary outcomes will be as follows: (1) 11-point (0-10) numeric rating scale (NRS) pain score immediately before surgery starts and after surgery; (2) degree of preserved diaphragmatic function (DPDF): the ratio of postoperative to pre-block (baseline) diaphragmatic excursion amplitude will be assessed in the holding area using a curvilinear probe (Sono Site, Transportable fuji M-turbo ultrasound system).;(3) degree of preserved handgrip strength (DPHS): the ratio of postoperative to pre-block (baseline) handgrip strength (the maximal force patients exerted when instructed to squeeze the dynamometer handles as tightly as feasible). Measurements will be done before surgery, immediately postoperative, 4, 8, and 24 hours postoperatively.
And (4) Recording of the complications which are: Hematoma, nerve injury, allergy to any of the used drugs.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Cairo, Egypt
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ultrasound guided anterior glenoid nerve block combined with Sub-omohyoid Anterior Suprascapular nerve Block
Ultrasound guided interscalene brachial plexus block
Time frame: 24 hours postoperative.
degree of preserved diaphragmatic function (DPDF): the ratio of postoperative to pre-block (baseline) diaphragmatic excursion amplitude will be assessed in the holding area using a curvilinear probe (Sono Site, Transportable fuji M-turbo ultrasound system).). Measurements will be made before surgery, immediately postoperative, 4, 8, and 24 hours postoperatively.
Ain Shams University
Other
A Comparative Study Between Ultrasound Guided Anterior Glenoid Block Combined With Sub-omohyoid Anterior Suprascapular Block Versus Ultrasound Guided Interscalene Block in Diagnostic Shoulder Arthroscopy
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06092502
Arthralgia, Joint Diseases
Istanbul, Turkey, Turkey (Türkiye)
View Trial DetailsNCT07291843
Arthralgia, Impingement Shoulder
Istanbul, Beykoz, Turkey (Türkiye)
View Trial DetailsNCT07261007
Arthralgia, Hemiplegia
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT07720050
Arthralgia, Core Endurance
Istanbul, Turkey (Türkiye)
View Trial Details