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NCT02006355 Clinical Trial

Continuous Local Anesthesia Versus Continuous Femoral Nerve Bloc After Total Knee Arthroplasty: Impact on Mean Discharge Aptitude Delay

Total Knee Arthroplasty Clinical Trial

— GLASGOW  

Official title:
Continuous Local Anesthesia Versus Continuous Femoral Nerve Bloc After Total Knee Arthroplasty: Impact on Mean Discharge Aptitude Delay

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02006355
Other study ID # 5560
Secondary ID
Status Terminated
Phase Phase 4
First received
Last updated
Start date April 2014
Est. completion date August 12, 2017

Study information
Verified date August 2018
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims at comparing continuous local anesthesia and femoral nerve bloc for total knee arthroplasty in terms of post-operative recovery.

Recruitment information / eligibility
Status Terminated
Enrollment 36
Est. completion date August 12, 2017
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Total knee arthroplasty

- Age > 18 years with social security covering.

- Written informed consent

Exclusion Criteria:

- Age < 18 years

- ASA Physical Status > III

- Body weight < 50 kg

- Latex or silver allergy.

- Loco-regional anesthesia contraindication

- Chronic anticoagulant, corticoid or pain treatment.

- Rivaroxaban or enoxaparin contraindication

- Communication issues

- Patient under guardianship

- Pregnant or breast-feeding patient

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Ropivacaine

Locations
Country Name City State
France CCOM-Hôpitaux Universitaires de Strasbourg Illkirch-Graffenstaden

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Discharge ability time period Participants will be followed for the duration of hospital stay, an expected average of 10 days
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