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The Comparison of Local Infiltration Analgesia versus Adductor canal block on Postoperative pain and Functional outcome after Total knee replacement: A randomized clinical trial

The Comparison of Local infiltration analgesia and Adductor canal block on postoperative pain and Functional outcome after Total knee replacement

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20150720003
Enrollment
Unknown
Registered
2015-07-20
Start date
2015-07-21
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Osteoarthritis Knee Total knee arthroplasty Postoperative TKA analgesia adductor canal block Total knee arthroplasty Postoperative analgesia functional outcome single shot adductor canal block local infiltration analgesia

Interventions

0.5%levobupivacaine 20 ml+morphine 5 mg.+ adrenaline (1 : 1&#44
000) 0.3 ml + normal saline up to 60 ml inject at anterior&#44
medial&#44
lateral and supra&#45
patella pouch of the knee&#44
before insertion of prosthetic instruments and before suture surgical wound.,single shot adductor canal block under high frequency linear ultrasound&#44
by 22 gauge 100 mm. stimuplex&#45
0.5%levobupivacaine 20 ml was injected at recovery room.
Active Comparator Drug,Active Comparator Drug
local infiltration analgesia after total knee arthroplasty,single shot adductor canal block

Sponsors

Research Affairs Faculty of medicine, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patient aged > 18 years old, who was scheduled for total knee arthroplasty American Society of anesthesiologist class 1-3 Patient BMI 18-40 kg/m2

Exclusion criteria

Exclusion criteria: refuse to participate this study allergy to any drug in this study age 3 BMI 40 kg/m2 contraindication to neuraxial anesthesia uncontrolled hypertension or Blood pressure greater than 140/90 mmmHg history of heart failure, cerebrovascular disease, cardiac surgery, coronary artery disease history of upper GI bleeding, gastric ulcer history of abnormal liver enzyme, hepatic failure, renal failure, organ transplantation, coagulopathy chronic opioids user defined as using opioids drug almost/everyday for three consecutive months or more than 60 mg/day for one month neuropathic pain failure to single shot adductor canal block inability to cooperate with Time Up and Go Test before surgery

Design outcomes

Primary

MeasureTime frame
morphine consumption postoperative 24 hours postoperative 24 hr mg of morphine consumption using PCA device

Secondary

MeasureTime frame
degree of knee flexion(active and passive) postoperative day1,2,3 postoperative day 1, 2, 3 degree of range of motion,morphine consumption postoperative 48 hours postoperative 48 hr mg of morphine consumption using PCA device,Pain score postoperative 6,12,18 hours postoperative 6,12,18 hours visual analog scale,pain score at rest, sit, flexion, extension of the knee postoperative postoperative day 1 in the morning and evening visual analog scale,pain score at rest, sit, stand, walk postoperative postoperative day 2,3 visual analog scale,Quadriceps strength postoperative day 1, 2, 3 postoperative day 1, 2, 3 maximum voluntary isometric contraction,rehabilitation after surgery on postoperative day 3 The Timed Up and Go test (TUG),pain score postoperative 2,6,12 weeks postoperative 2,6,12 weeks visual analog scale,rehabilitation after surgery postoperative 2,6,12 weeks The Timed Up and Go test (TUG)

Countries

Thailand

Contacts

Public ContactWireena Kampitak

unaffiliated

nutong127@yahoo.com6689-9955-666

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026