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

NCT ID: NCT04189198

Last Updated: 2020-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-12-30

Study Completion Date

2020-03-27

Brief Summary

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

Detailed Description

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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

Conditions

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Upper Limb Surgery Hand Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Articaine group

Patients in this group are assigned to recieve 30 ml of Articaine 2%

Group Type EXPERIMENTAL

Articaine

Intervention Type DRUG

Supraclavicular block with 30 ml articaine 2%

Bupivacaine

Patients in this group are assigned to recieve 30 ml of bupivacaine 0.5%

Group Type EXPERIMENTAL

Bupivacaine

Intervention Type DRUG

Supraclavicular block with 30 ml bupivacaine 0.5%

Interventions

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Articaine

Supraclavicular block with 30 ml articaine 2%

Intervention Type DRUG

Bupivacaine

Supraclavicular block with 30 ml bupivacaine 0.5%

Intervention Type DRUG

Other Intervention Names

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Artinebsa Marcaine

Eligibility Criteria

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Inclusion Criteria

* upper limb surgery
* ganglion removal
* k wiring
* Carapal tunnel

Exclusion Criteria

* Coagulopathy.
* infection at site of injection.
* patient refusal.
* hypersensitivity.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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simon Halim Armanious

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Galal Mo El kadi, Doctor

Role: STUDY_DIRECTOR

Professor

Locations

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Ain Shams University hosptal

Cairo, Abbasya, Egypt

Site Status

Countries

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Egypt

References

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Armanious SH, Abdelhameed GA. A Randomized Controlled Trial: Comparison of 4% Articaine versus 0.5% Bupivacaine for Ambulatory Orthopedic Surgery under Supraclavicular Block. Anesthesiol Res Pract. 2020 Sep 24;2020:2194873. doi: 10.1155/2020/2194873. eCollection 2020.

Reference Type DERIVED
PMID: 33029135 (View on PubMed)

Other Identifiers

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Articaine versus bupivacain

Identifier Type: -

Identifier Source: org_study_id

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