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A Comparison of Adductor canal block with or without Local infiltration analgesia after Total knee arthroplasty: A Randomized controlled trial

A Comparison of Adductor canal block with or without Local infiltration analgesia after Total knee arthroplasty: A Randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20150720006
Enrollment
62
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

postoperative pain score postoperative morphine consumption rehabilitation after surgery adductor canal block Randomized Controlled Trial Aged Analgesia&#44

Interventions

patient will receive single shot adductor canal block under ultrasound&#45
guided using 0.5% levobupivacaine 20 ml combine with local infiltration analgesia using 0.25% levobupivacaine 80 ml&#44
morphine 5 mg and adrenaline 300 mcg.,patient will receive single shot adductor canal block under ultrasound&#45
guided using 0.5% levobupivacaine 20 ml combine with local infiltration using normal saline 80 ml.
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
single shot adductor canal block combined with local infiltration analgesia,single shot adductor canal block alone

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: age > 18 years ASA physical status 1-3 no contraindication of neuraxial anesthesia

Exclusion criteria

Exclusion criteria: refuse to participate this study allergy to drug using in this study age 3 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 opiod user defined as using opiods 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
Rehabilitation after surgery on postoperative day 2 The Timed Up and Go test (TUG)

Secondary

MeasureTime frame
morphine consumption postoperative 24 hours postoperative 24 hours mg of morphine consumption using PCA device,morphine consumption postoperative 48 hours postoperative 48 hours 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 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,degree of knee flexion(active and passive) postoperative postoperative day2,3 degree of range of motion,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),Quadriceps strength postoperative day1,2 postoperative day 2,3 maximum voluntary isometric contraction

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