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Comparison of femoral nerve block with posterior capsule infiltration versus anterior and posterior capsule infiltration after total knee replacement.

Comparison of femoral nerve block with posterior capsule infiltration versus anterior and posterior capsule infiltration after total knee replacement. - LiFeAnKeR

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON42184
Enrollment
90
Registered
2015-03-31
Start date
2015-03-01
Completion date
Unknown
Last updated
2025-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

mobility Pain

Interventions

Patients in the SFNB group will get a femoral nerve block with ropivacaine 0,375% and 75 microgram clonidine, and furthermore will recieve 50cc ropivacaine 0,2% with epinephrine 1:100.000 in the pos

Sponsors

Sint Lucas Andreas Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients 18 years and older who are scheduled for a TKA with spinal anesthesia. ;- age above 18 years ;- mentally competent;- eligible for TKA;- informed consent

Exclusion criteria

Exclusion criteria: -contra indication for spinal anesthesia (severe aortic stenosis, severely compromised cardiac function);- infection at interspace of spinal injection;- allergy to used medicine;- repeat TKA;- all previous surgeries concerning arthrotomy;- participation in other research protocol

Design outcomes

Primary

MeasureTime frame
-Opioid consumption measured by mg of morphine i.v. used daily (every morning at 10.00 am by painconsulent and/or researcher) -Mobilization measured by Modified Iowa Levels of Assistance Scale (MILAS)

Secondary

MeasureTime frame
- NRS pain score in rest from the day of surgery until day 3 post surgery - NRS pain score in flexion exercise from the day of surgery until day 3 post surgery - NRS pain score postoperatively when walking - range of motion with flexion and extension during 3 postoperative days - length of stay in hospital - side-effects

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)