jRCT1030250650Not yet recruitingNot Applicable
A double-blind randomized controlled trial to evaluate the efficacy of combined femoral nerve block and selective tibial nerve block for postoperative pain management in high tibial osteotomy.
Not provided0 sites60 target enrollmentStarted: TBD
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
Eligibility Criteria
- Ages
- 20age old over to No limit (—)
- Sex
- All
Inclusion Criteria
- •Patients undergoing medial open wedge high tibial osteotomy at our hospital.
- •Patients over 20 years
- •Patients who receive written informed consent.
- •Patients with American Society of Anesthesiologists physical status classification 1-3.
Exclusion Criteria
- •Patients who are deemed inappropriate as research subjects by the principal investigator
- •Patients who refuse to participate in the study.
- •Patients who have contraindications to the use of usual postoperative analgesics such as NSAIDs and acetaminophen, contraindications to local anesthetics, are pregnant or suspected pregnant women, poorly controlled diabetes, unable to understand the perioperative questionnaire (language or cognitive impairment), severe heart disease, Severe obesity (BMI > 35), patients who have not responded to nerve blocks, emergency surgery.
Investigators
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