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Clinical Trial Summary

The patients will be randomly allocated into two equal groups (each 20 patients) using sealed opaque numbered envelopes: Control Group (C Group) : Patients receive continuous US suprascapular nerve block only. Gabapentin Group (G Group) : Patients receive continuous US suprascapular nerve block with oral gabapentin 300 mg once daily at bed time. Both groups compared as regard: Visual Analogue Scale Range of passive and active movements Patients satisfaction complication related to block The total dose of diclofenac sodium


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05037994
Study type Interventional
Source Zagazig University
Contact AMR SH ELSHAFEI, MD
Phone 01225800795
Email [email protected]
Status Recruiting
Phase N/A
Start date April 1, 2021
Completion date October 2021

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