Ain Shams University hosptal
Cairo, Abbasya, Egypt
NCT Number: NCT04189198
Effect of 2%Articaine versus 5%bupivacaine in pt undergoing short duration surgery in upper limb
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Notify Me18 year–75 year
All sexes
Interventional
Phase 1
Cairo, Abbasya, Egypt
The investigator aim to compare Articaine 2% versus bupivacaine 0.5% in patient undergoing upper limb procedure under ultrasound guided supraclavicular block as regard onset and duration of sensory and motor block
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Supraclavicular block with 30 ml articaine 2%
Other names: Artinebsa
Supraclavicular block with 30 ml bupivacaine 0.5%
Other names: Marcaine
Time frame: Measured in minutes over 24 hours
By pinprick test from 0 to 2 where 0 no sensory block and 2 complete anesthesia
Time frame: Measured in minutes over 24 hours
By Bromage scale from 1 to 4 where 1 no motor power and 4 full motor power
Time frame: Measured in minutes over 24 hours
Measured by numerical analog scale where 0 no pain and 10 means worst pain
Time frame: 24 hours
First analgesia required
Ain Shams University
Other
A Randomized Controlled Trial : Comparison of 4% Articaine Versus 0.5% Bupivacaine for Ambulatory Orthopaedic Surgery Under Supraclavicular Block
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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.
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