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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00403013
Other study ID # 01-AnIt-06
Secondary ID
Status Completed
Phase N/A
First received November 22, 2006
Last updated July 3, 2009
Start date April 2007
Est. completion date June 2009

Study information

Verified date July 2009
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 determine whether the axillary plexus block performed in lateral, head down position is effective in the perioperative analgesia in patients scheduled for elective surgery of the shoulder.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date June 2009
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients scheduled for elective surgery of the shoulder

Exclusion Criteria:

- lateral, head down position not possible

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Positioning and anesthesia
Positioning during axillary plexus block

Locations

Country Name City State
Germany Department of Anesthesiology and Intensive Care, University Hospital Muenster Muenster

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Muenster

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Orlowski O, Bullmann V, Vieth V, Filler T, Osada N, Van Aken H, Weber TP. Perivascular axillary brachial plexus block and patient positioning: the influence of a lateral, head-down position. Anaesthesia. 2006 Jun;61(6):528-34. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scale (VAS) score 8 hours after start of axillary plexus block No
Primary VAS Score 24 hours after start of axillary plexus block No
Secondary Opioid consumption intraoperatively No
Secondary Patient comfort six months after surgery No
Secondary Opioid consumption during hospital stay No
See also
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Completed NCT05772533 - Serratus Anterior Plane Block Versus Pericapsular Nerve Group Block for Shoulder Surgery N/A
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Completed NCT05755802 - Shoulder Block Versus Pericapsular Nerve Group Block for Shoulder Surgery N/A
Completed NCT01185457 - Effect of Interscalene Block on Heart Rate Variability (HRV) N/A
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Withdrawn NCT02435251 - Changes in Anthropometry Following Ambulatory Orthopaedic Surgery
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Completed NCT04714112 - Low-dose Intravenous Dexamethasone at Different Times as Adjunvants for Brachial Plexus Blocks Phase 4
Completed NCT04769570 - Effect of Interscalene and Suprascapular Nerve Block on Analgesia Consumption After Adhesive Capsulitis Surgery N/A
Completed NCT02074397 - Distant Extrafascial Injection vs Subfascial Injection for Interscalene Block: Acute Pain Outcomes and Rates of Complications N/A
Recruiting NCT03664284 - Does the Disinfection of the Subcutaneous Tissue Reduce the Contamination of the Operative Field by P. Acnes During Primary Shoulder Surgery? N/A