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NCT01875289 Clinical Trial

Efficacy of a Modified Obturator Nerve Block Technique

Hip Surgery Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01875289
Other study ID # VOB-Studie EK 25-387 ex 12/13
Secondary ID
Status Completed
Phase N/A
First received June 7, 2013
Last updated March 20, 2014
Start date July 2013

Study information
Verified date March 2014
Source Medical University of Graz
Contact n/a
Is FDA regulated No
Health authority Austria: Federal Office for Safety in Health Care
Study type Interventional

Clinical Trial Summary

Efficacy of a modified obturator nerve block technique by using only a single morphological landmark, a double-blinded randomised pilot study.

Recruitment information / eligibility
Status Completed
Enrollment 36
Est. completion date
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- American Society of Anesthesiologists 1-3, older than 18 y, cooperative patient

Exclusion Criteria:

- infection, neuromuscular deficits of the lower extremities,pregnancy, neurologic disease

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• obturator nerve block

Locations
Country Name City State
Austria Medical University Graz Graz

Sponsors (1)
Lead Sponsor Collaborator
Medical University of Graz

Country where clinical trial is conducted

Austria, 

References & Publications (1)

Feigl GC, Ulz H, Pixner T, Dolcet C, Likar R, Sandner-Kiesling A. Anatomical investigation of a new vertical obturator nerve block technique. Ann Anat. 2013 Jan;195(1):82-7. doi: 10.1016/j.aanat.2012.05.008. Epub 2012 Aug 10. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Adductor strengths Adductor muscle strength is measured with a sphygmomanometer. Patients are instructed to squeeze a blod pressure cuff, already inflated to 40 mm Hg, between their extended knees. The maximal sustained pressure is taken as the baseline adductor strength. pre operative, 30 minutes before start surgery No
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