NCT01409460|Completed
Obturator Nerve Block With Femoral and Sciatic Block
Is an Obturator Nerve Block Required for Every Patient Having Total Knee Arthroplasty With Femoral and Sciatic Nerve Block?
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Is an Obturator Nerve Block Required for Every Patient Having Total Knee Arthroplasty With Femoral and Sciatic Nerve Block?
Sponsor study identifier
interventional
16
1 country
1
Study Start
October 2008
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
June 2009
Actual (reported)Study Completion
July 2009
Actual (reported)The purpose of this study is to evaluate how many patients require the addition of the obturator nerve block in the recovery room after the total knee surgery. Also to study the efficacy of blocking the obturator nerve in controlling their knee pain.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
July 2009
Actual (reported)Click on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
October 2008
Date type not reportedThis date has not been verified as actual or estimated.
June 2009
Actual (reported)July 2009
Actual (reported)August 2, 2011
Actual (reported)August 4, 2011
Actual (reported)To assess the use of obturator Nerve block for patients undergoing total knee arthroplasty
The need for rescue obturator nerve block in total knee arthoplasty patients who have sucessful femoral nerve block and sciatic nerve block in place.
15 minutes in recovery room post operatively
Pain medication use intra-operatively and in the recovery room after surgery. Pain scores in recovery room.
During surgery and until discharge from recovery room.
Use of selective pain block.
Five minutes after the sham block pain was assessed in these patients. If pain score was 5 or greater a true obturator nerve block was performed on these patients.
Saint Francis Hospital and Medical Center
Hartford, Connecticut, 06105, United States
16 participants (actual enrollment reported by the registry).
First Submitted
August 2, 2011
First Posted
August 4, 2011
Study Start
October 2008
Date type not reportedThis date has not been verified as actual or estimated.
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Contact the study team to confirm eligibility.
Primary Completion
June 2009
Actual (reported)Study Completion
July 2009
Actual (reported)Last Updated
August 4, 2011
Record last verified: 2008-10
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Source: ClinicalTrials.gov.
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