Shoulder Surgery Clinical Trial
Official title:
Axillary Plexus Block for Perioperative Analgesia in Patients Scheduled for Elective Surgery of the Shoulder: Influence of Lateral, Head-Down Position
Verified date | July 2009 |
Source | University Hospital Muenster |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Ethics Commission |
Study type | Interventional |
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.
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 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Germany | Department of Anesthesiology and Intensive Care, University Hospital Muenster | Muenster |
Lead Sponsor | Collaborator |
---|---|
University Hospital Muenster |
Germany,
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
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 |
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