Comparison Between Two Different Volumes of Anesthesia Drug in Forearm Surgery

Comparison of Axillary Block Under Ultrasound With 40 or 25 ml of Xylocaine 1.5% Adrenalin in Forearm or Arm Surgery.

Status

Completed

Phases

Phase 3

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01216488

Acronym

COMBAX

Enrollment

Registered

2010-10-07

Start date

2010-01-31

Completion date

2011-06-30

Last updated

2011-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Forearm and Arm Surgery

Keywords

Forearm surgery, Hand surgery, Anesthesia

Brief summary

Hospitalized patients for superior member surgery have different types of anesthesia.Forearm and/or arm surgery could be done under general anesthesia, but in the most of the cases, this surgery was done under locoregional anesthesia.Several injections of local anesthesia at the nerves axilla are used with the used of ultrasonography. The purpose of this study is to show that the anesthesia efficiency is the same with 40 or 25 ml of Xylocaine 1.5% Adrenalin in Forearm or Arm Surgery.

Detailed description

Inclusion criteria : * age \> 18 years old * patient who must have a non emergency surgery of the forearm or the hand * ASA I or ASA II * informed consent * Ensured patient Exclusion criteria : * pregnancy * respiratory insufficiency * cardiac insufficiency * hepatic insufficiency * renal insufficiency * ASA III or IV * contraindications to the locoregional anesthesia * contraindications to the xylocaine used * patient participate to an another clinical study * guardianship patient

Interventions

DRUGXylocaine

40 ml or 25 ml of Xylocaine injection

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* age \> 18 years old * patient who must have a non emergency surgery of the forearm or the hand * ASA I or ASA II * informed consent * Ensured patient

Exclusion criteria

* pregnancy * respiratory insufficiency * cardiac insufficiency * hepatic insufficiency * renal insufficiency * ASA III or IV * contraindications to the locoregional anesthesia * contraindications to the xylocaine used * patient participate to an another clinical study * guardianship patient

Design outcomes

Primary

Measure	Time frame	Description
Axillary block efficiency conducted by ultrasound	48 hours	during the hospitalisation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026