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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00151112
Other study ID # 01-Anast-05
Secondary ID
Status Completed
Phase N/A
First received September 7, 2005
Last updated September 10, 2008
Start date September 2005
Est. completion date August 2008

Study information

Verified date September 2008
Source University Hospital Muenster
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Single shot axillary block

Exclusion Criteria:

- Lateral position not possible

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
Positioning and plexus anesthesia
positioning during plexus anesthesia

Locations

Country Name City State
Germany Department of Anesthesiology and Intensive Care, University Hospital Münster Münster
Germany BG Unfallklinik Murnau; Department of Anesthesiology Murnau

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Muenster

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Bullmann V, Waurick R, Rödl R, Hülskamp 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. German. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Extent of anesthesia 20 minutes after acillary plexus block Yes
Primary Efficacy of anesthesia 20 minutes after axillary plexus block No
Secondary Rate of failure 20 minutes after axillary plexus block No
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