NCT00151112

Brief Summary

The purpose of this study is to investigate the influence of difference positioning on extension and efficacy of brachial plexus anesthesia at 20 minutes by using the axillary plexus block with supine positioning and a lateral positioning onto the non-anaesthetized side, combined with 20° Trendelenburg positioning.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2005

Typical duration for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2005

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

September 7, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 8, 2005

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2008

Completed
Last Updated

September 11, 2008

Status Verified

September 1, 2008

Enrollment Period

2.9 years

First QC Date

September 7, 2005

Last Update Submit

September 10, 2008

Conditions

Wounds and Injuries

Keywords

nerve blockregional anesthesiainjuriesdiverse malformations

Outcome Measures

Primary Outcomes (2)

  • Extent of anesthesia

    20 minutes after acillary plexus block

  • Efficacy of anesthesia

    20 minutes after axillary plexus block

Secondary Outcomes (1)

  • Rate of failure

    20 minutes after axillary plexus block

Study Arms (2)

1

EXPERIMENTAL

combination of lateral position and 20° Trendelenburg Position

Procedure: Positioning and plexus anesthesia

2

ACTIVE COMPARATOR

standard positioning

Procedure: Positioning and plexus anesthesia

Interventions

Positioning and plexus anesthesiaPROCEDURE

positioning during plexus anesthesia

12

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Single shot axillary block

You may not qualify if:

  • Lateral position not possible

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

BG Unfallklinik Murnau; Department of Anesthesiology

Murnau am Staffelsee, D-82418, Germany

Location

Department of Anesthesiology and Intensive Care, University Hospital Münster

Münster, D-48149, Germany

Location

Related Publications (1)

  • Bullmann V, Waurick R, Rodl R, Hulskamp G, Orlowski O, van Aken H, Winkelmann W, Weber TP. [Corrective osteotomy of the humerus using perivascular axillary anesthesia according to Weber in a patient suffering from McCune-Albright syndrome]. Anaesthesist. 2005 Sep;54(9):889-94. doi: 10.1007/s00101-005-0874-6. German.

    PMID: 15947897BACKGROUND

MeSH Terms

Conditions

Wounds and Injuries

Interventions

Patient Positioning

Intervention Hierarchy (Ancestors)

Patient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and Services

Study Officials

  • Thomas Weber, MD

    Department of Anesthesiology and Intensive Care, University Hospital Münster

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 7, 2005

First Posted

September 8, 2005

Study Start

September 1, 2005

Primary Completion

August 1, 2008

Study Completion

August 1, 2008

Last Updated

September 11, 2008

Record last verified: 2008-09

Locations

DE(2)