Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04778774
Other study ID # KMUHIRB-F(I)-20200031
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 24, 2021
Est. completion date November 29, 2021

Study information

Verified date February 2021
Source Kaohsiung Medical University Chung-Ho Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Adductor canal block and femoral nerve block are the most commonly used nerve blocks for pain control after total knee arthroplasty. The block area for adductor canal is a sensory branch near the knee area, which can potentially reduce the effect of motor blockage of quadriceps muscle. We try to proof adductor canal block can reduce the pain level after surgery effectively and preserve the muscle power of quadriceps muscle. Therefore, the rehabilitation course can be reduced and further lowering the risks of falling and complications.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date November 29, 2021
Est. primary completion date October 18, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 100 Years
Eligibility Inclusion Criteria: - Age at least 50 years old, not exceed 100 years old - Diagnosed Primary Knee Osteoarthritis - Accepted Total Knee Arthroplasty Exclusion Criteria: - Diagnosed Osteonecrosis - Diagnosed inflammatory Arthritis?Rheumatoid Arthritis - Accepted Revision Total Knee Arthroplasty - Quadriceps muscle rupture, suture or repair history - Neurological or orthopedic disorders that could affect quadriceps muscle power - Allergy to amide anesthetics - Patients who cannot obey or follow directions

Study Design


Related Conditions & MeSH terms

  • Quadriceps Function Monitored With Electromyography

Intervention

Procedure:
Nerve block
Two different nerve block types, Adductor canal block group and Femoral nerve block group

Locations

Country Name City State
Taiwan Kaohsiung Municipal Ta-Tung Hospital Kaohsiung

Sponsors (1)

Lead Sponsor Collaborator
Kaohsiung Medical University Chung-Ho Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quadriceps muscle Electromyography voltage level change before and after nerve block surface electromyography level compare difference of Quadriceps muscle Electromyography voltage level 12 weeks after surgery,data were measured post operation day 1, day 2, day 5, 2 weeks, 6 weeks and 12 weeks