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The Effect of a Prolonged Peripheral Nerve Block on the Level of Pain After a Knee Replacement

Not Applicable
Not yet recruiting
Conditions
Knee Replacement Surgery
Interventions
Drug: Continues peripheral block
Registration Number
NCT06382285
Lead Sponsor
Assaf-Harofeh Medical Center
Brief Summary

The aim of this study is to examine the effect of a prolonged peripheral nerve block (utilizing continuous adductor canal block) on the level of pain after a knee replacement surgery

Detailed Description

Knee replacement surgery is one of the common orthopedic surgeries for the treatment of chronic knee pain. The period after knee replacement surgery is accompanied by moderate to severe pain that affects the patient's ability to quickly return to function. Peripheral nerve blockers and analgesia of different types, administered as part of the anesthesia process, are optimal in controlling pain after surgery. After the surgery, the patients are admitted in the orthopedic inpatient department for 2-3 days on average after surgery for follow-up and early physical therapy necessary to achieve good results and return the patient to full function as soon as possible. The level of pain greatly affects the success rate of the patient's rehabilitation. Thus, since the duration of peripheral nerve block activity does not exceed 8-16 hours on average, it is suggested to treat the patients with a prolonged peripheral nerve block (utilizing continuous adductor canal block) for 24 hours after surgery.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Female and male patients between the ages of 18 and 80 who have signed an informed consent form.
  • ASA is less than 3
  • Spinal anesthesia
Exclusion Criteria
  • Patients with sensitivity to the anesthetic.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Treatment groupContinues peripheral blockropivacaine (Naropin) 0.2% according to a protocol 8-10 cc per hour up to 24 hours after the surgery
Control groupContinues peripheral blockSaline according to a protocol 8-10 cc per hour up to 24 hours after the surgery
Primary Outcome Measures
NameTimeMethod
Pain levelduring hospitalization (1-2 days)

Documentation of pain level during the hospitalization days every 12 hours (on a scale of 1-10)

Analgesic useduring hospitalization (1-2 days)

Documentation of pain level during the hospitalization days every 12 hours (on a scale of 1-10).

Documentation of analgesic administration in hospitalization.

Secondary Outcome Measures
NameTimeMethod
Physiotherapyduring hospitalization (1-2 days)

Documentation of the execution of a full or partial physical therapy program

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