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NCT01843153 Clinical Trial

Continuous Versus Intermittent Sciatic Block for Total Knee Arthroplasty

Pain Clinical Trial

Official title:
Continuous Versus Intermittent Sciatic Block Combined With a Continuous Femoral Block for Patients Undergoing Total Knee Arthroplasty: a Prospective, Randomized Trial.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01843153
Other study ID # sciatic block
Secondary ID
Status Completed
Phase Phase 4
First received April 25, 2013
Last updated March 30, 2015
Start date April 2013
Est. completion date December 2014

Study information
Verified date April 2013
Source Kreiskrankenhaus Dormagen
Contact n/a
Is FDA regulated No
Health authority Ethics commission Germany: Aerztekammer Nordrhein, Duesseldorf
Study type Interventional

Clinical Trial Summary

The role of a sciatic block in addition to a femoral block remains controversial. The study addresses this topic by comparing a continuous block versus an injection on demand.

Recruitment information / eligibility
Status Completed
Enrollment 140
Est. completion date December 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients scheduled for total knee arthroplasty

Exclusion Criteria:

- failure to establish femoral and sciatic block

- insufficient analgesic effect of the block

- patient declines to participate

Study Design

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

Related Conditions & MeSH terms

Intervention

Drug:
• Ropivacaine

Locations
Country Name City State
Germany KKH Dormagen Dormagen

Sponsors (1)
Lead Sponsor Collaborator
Kreiskrankenhaus Dormagen

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain score (VRS) 4 days No
Secondary frequency of injections into the sciatic catheter 4 days No
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