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The Appropriate Level of Continuous Adductor Canal Block in Patients Undergoing Total Knee Arthroplasty (TKA)

The Appropriate Level of Continuous Adductor Canal Block in Patients Undergoing Total Knee Arthroplasty (TKA)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04206150
Enrollment
96
Registered
2019-12-20
Start date
2020-04-02
Completion date
2021-07-17
Last updated
2021-10-15

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

Conditions

Degenerative Arthritis

Brief summary

Adductor canal catheters are being used to provide continuous postoperative analgesia after total knee arthroplasty surgery (TKA). There is much debate about where is the best position of continuous adductor canal block in patients undergoing TKA. Therefore, the investigators aim to compare the postoperative pain at three different level of continuous adductor canal block. Ninety six patients scheduled for total knee arthroplasty will be randomly divided into the three groups. In group 1, the adductor canal catheter is inserted at femoral triangle apex (the proximal end of the adductor canal). In group 2, the adductor canal catheter is inserted femur length/15\*2 cm above the location where the nerve block performed in group 1. In group 3, the adductor canal catheter is inserted femur length/15cm below the location where the nerve block performed in group 1.

Interventions

PROCEDUREthe three different sites of continous adductor canal block: the adductor canal catheter is inserted at femoral triangle apex

In group 1, the adductor canal catheter is inserted at femoral triangle apex (the proximal end of the adductor canal).

PROCEDUREthe three different sites of continous adductor canal block: the adductor canal catheter is inserted femur length/15*2 cm above the location

In group 2, the adductor canal catheter is inserted femur length/15\*2 cm above the location where the nerve block performed in group 1.

PROCEDUREthe three different sites of continous adductor canal block: the adductor canal catheter is inserted femur length/15 cm below the location

In group 3, the adductor canal catheter is inserted femur length/15 cm below the location where the nerve block performed in group 1.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Investigator and outcomes assessor are blinded to group assignment.

Intervention model description

Ninety six patients scheduled for total knee arthroplasty will be randomly divided into the three groups. In group 1, the adductor canal catheter is inserted at femoral triangle apex (the proximal end of the adductor canal). In group 2, the adductor canal catheter is inserted femur length/15\*2 cm above the location where the nerve block performed in group 1. In group 3, the adductor canal catheter is inserted femur length/15\*2 cm below the location where the nerve block performed in group 1.

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 1\. Patients undergoing total knee arthroplasty

Exclusion criteria

* 1\. Patients who have infection or had surgery on the thigh * 2\. The subject is a foreigner or illiterate * 3\. Patients who have cognitive dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Pain : Visual Analogue Scale (VAS) for painBaseline (Before surgery)The visual analog scale(VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between no pain (0) and worst pain. (10). The ends are defined as the extreme limits of the parameter to be measured(symptom,pain,health) orientated from the left(0, worst) to the right(10, best).

Secondary

MeasureTime frameDescription
muscle strengthBaseline (Before surgery)Quadriceps strength of both legs was assessed by placing the dynamometer on the anterior of the ankle, between the malleoli.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026