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Selective Tibial Nerve Block vs Local Infiltration Analgesia After Prothetic Knee Surgery

Optimal Pain Control After Prothetic Knee Surgery Either by Selective Tibial Nerve Block Versus Local Infiltration Analgesia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03698006
Enrollment
60
Registered
2018-10-05
Start date
2021-02-12
Completion date
2022-06-30
Last updated
2022-10-10

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

Conditions

Knee Osteoarthritis, Postoperative Pain

Brief summary

Patient suffer from moderate posterior knee pain after TKA despite injection of local anesthetic around the femoral or saphenous nerves. Indeed, the posterior part of the knee is innervated by the sciatic nerve. This nerve is not routinely blocked as clinicians fear to produce a motor block of the leg that might impair the postoperative assessment. An analgesic alternative is the infiltration of the knee with local anesthetics performed by the surgeon. Recently a trial(1) demonstrated that a selective tibial nerve block provides an effective analgesia without a motor blockage when compared with a sciatic nerve block. The objective of this randomized controlled double-blinded trial is to assess whether a tibial nerve block is more effective for the postoperative pain than local infiltration analgesia when there are combined with an adductor canal block, without decreasing the functional parameters.

Interventions

DRUGRopivacaine 0.5% Injectable Solution

Tibial nerve block with 10ml of Ropivacaine 0.5%

DRUGRopivacaine 0.2% Injectable Solution

Infiltration with 25ml of Ropivacaine 0.2% in the posterior knee capsule

Sponsors

Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient scheduled for a total knee arthroplasty under spinal block. * Patient with a weight above 40kg.

Exclusion criteria

* Patient with ASA IV status. * Contraindication to spinal block, or peripheral nerve blocks. * Neurological deficit of the lower limb. * Patient with renal dysfunction. * Patient with chronic pain, opioid consumption or alcohol consumption. * Pregnancy.

Design outcomes

Primary

MeasureTime frame
Total morphine consumption (mg)24 hours postoperatively

Secondary

MeasureTime frameDescription
Pain scores (numeric rating scale, 0-10) at rest and on movement2 hours, 24 hours, 48 hours and 72 hours postoperatively0= no pain, 10=the worst pain imaginable
Rate of postoperative nausea and vomiting2 hours, 24 hours, 48 hours and 72 hours postoperativelyYes/No
Rate of prurit2 hours, 24 hours, 48 hours and 72 hours postoperativelyYes/No
Total morphine consumption (mg)2 hours, 48 hours and 72 hours postoperatively
Analgesic duration (minutes)Postoperative day 0Time from the block to the first analgesic request
Active flexion24hours, 48hours and 72hours postoperativelyFlexion of the knee by the patient measured in degrees
Quadriceps muscle strength (numeric scale, 1-5)24hours, 48hours and 72hours postoperatively1=no contraction, 5=normal strength
Distance walked (meters)24hours, 48hours and 72hours postoperatively
Complication of tibial nerve blockup to 1 weekIntravascular injection/hematoma/infection/Common peroneal nerve block
Length of stay in hospitalup to 14 daysDays
Passive flexion24hours, 48hours and 72hours postoperativelyFlexion of the knee by physiotherapist measured in degrees

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026