A Comparison of 4% Articaine Versus 0.5%Bupivacaine for Ambulatory Surgery Under Supraclavicular Block

Hand Surgery Clinical Trial

Official title:

A Randomized Controlled Trial : Comparison of 4% Articaine Versus 0.5% Bupivacaine for Ambulatory Orthopaedic Surgery Under Supraclavicular Block

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04189198
• Other study ID #: Articaine versus bupivacain
• Status: Completed
• Phase: Phase 1
• Start date: December 30, 2019
• Est. completion date: March 27, 2020

Study information

• Verified date: April 2020
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Effect of 2%Articaine versus 5%bupivacaine in pt undergoing short duration surgery in upper limb

Description:

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: March 27, 2020
• Est. primary completion date: March 22, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• upper limb surgery

• ganglion removal

• k wiring

• Carapal tunnel

Exclusion Criteria:

• Coagulopathy.

• infection at site of injection.

• patient refusal.

• hypersensitivity.

Related Conditions & MeSH terms

• Hand Surgery
• Upper Limb Surgery

Intervention

Drug:
• Articaine
Supraclavicular block with 30 ml articaine 2%
• Bupivacaine
Supraclavicular block with 30 ml bupivacaine 0.5%

Locations

Country	Name	City	State
Egypt	Ain Shams University hosptal	Cairo	Abbasya

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Duration of sensory block	By pinprick test from 0 to 2 where 0 no sensory block and 2 complete anesthesia	Measured in minutes over 24 hours
Primary	Durations of motor block	By Bromage scale from 1 to 4 where 1 no motor power and 4 full motor power	Measured in minutes over 24 hours
Primary	Duration of analgesia	Measured by numerical analog scale where 0 no pain and 10 means worst pain	Measured in minutes over 24 hours
Secondary	Analgesia	First analgesia required	24 hours