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Efficacy and Safety of Chuna Manual Treatment as an Adjunctive Therapy After Total Knee Arthroplasty: A Study Protocol for a Single-Center, Randomized, Assessor Blind, Parallel-Group Clinical Trial

Efficacy and Safety of Chuna Manual Treatment as an Adjunctive Therapy After Total Knee Arthroplasty: A Study Protocol for a Single-Center, Randomized, Assessor Blind, Parallel-Group Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03625050
Enrollment
22
Registered
2018-08-10
Start date
2018-11-01
Completion date
2021-05-31
Last updated
2021-07-08

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

Conditions

Manipulation, Total Knee Replacement

Brief summary

Evaluate the efficacy and safety of Chuna treatment as an adjunctive therapy in patients with moderate pain following total knee replacement.

Interventions

PROCEDUREChuna + Usual care(Celecoxib and esomeprazole)

Chuna therapy (CT), 2 sessions/week, 4 weeks (8 sessions in total) Usual care therapy (UC, Celecoxib 200mg, qd and esomeprazole 20mg, qd), 4 weeks Usual care consists of physical therapy, CP based medications and patients education. Physical therapy consists of meridian muscle interferential current electricity (or meridian transcutaneous electricity) and hot pack (or infrared lamp). CT and UC group will receive the same UC regimen.

DRUGUsual care(Celecoxib and esomeprazole)

Usual care therapy (UC, Celecoxib 200mg, qd and esomeprazole 20mg, qd), 4 weeks Usual care consists of physical therapy, CP based medications and patients education. Physical therapy consists of meridian muscle interferential current electricity (or meridian transcutaneous electricity) and hot pack (or infrared lamp).

Sponsors

Catholic Kwandong University
CollaboratorOTHER
Gachon University Gil Oriental Medical Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Patients with NRS of knee pain ≥4 during the 7 days after 3 months total knee replacement * Patients who have agreed to trial participation and provided written informed consent

Exclusion criteria

* Those who have been diagnosed with certain serious diseases that can cause knee pain. : tumor, infectious or inflammatory disease, etc. * Those taking analgesics for the purpose of relieving pain, fever and inflammation within 7 days * Those with progressive neurological deficits or with severe neurological symptoms * Those who have other chronic conditions that may interfere with the interpretation of treatment effects or outcomes : Cardiovascular disease, kidney disease, diabetic neuropathy, dementia, epilepsy, etc. * Those who are not fit or unsafe to chuna therapy: clotting disorders, Those receiving anticoagulant therapy, Severe diabetes patients who are at risk of infection, severe cardiovascular disease * Those who are participating in other clinical trials * Those who have a history of participating in other clinical trials within one month * Those who are difficult to write a research consent form * Those who are judged to be inappropriate for the clinical study by the researchers.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline K-WOMAC score at week 4Week 0, Week 4Assess the recovery of knee function

Secondary

MeasureTime frameDescription
Change from baseline EQ-5D score at every visitWeek 0, Week 2, Week 4, Week 8EQ-5D is a tool developed for health-related quality of life (HRQoL) assessment, and is widely used in the health care sector. Scores range from -1, 'health worse than death' to 1, 'perfect health'. EQ-5D-5L has 5 dimensions covering current health status and functionality: mobility (M), self care (SC), usual activities (UA), pain/discomfort (PD), and anxiety/depression (AD), to be rated out of 5 grades (1, no problem; 2, slight problem; 3, some/moderate problem; 4, severe problem; 5, extreme problem).
Change from baseline Numeric rating scale score at every visitWeek 0, Week 2, Week 4, Week 8In pain measurement using NRS, patients are asked to rate their pain by selecting a number from 0 to 10 that best represents their pain severity between the anchors of 0 which indicates 'no pain', and 10 which indicates 'worst pain possible'.
Change from baseline in Physical Condition related with mobility at every visitWeek 0, Week 2, Week 4, Week 8, Week 12mobility (5 meters walking test at comfortable speed - 5mWT) (meters/second)
Change from baseline in Physical Condition related with endurance at every visitWeek 0, Week 2, Week 4, Week 8, Week 12endurance (Sit-to-stand test - STS) (seconds)
Change from baseline K-WOMAC score at every visitWeek 0, Week 2, Week 4, Week 8Assess the recovery of knee function
Change from baseline in Alternative-Step Test at every visitWeek 0, Week 2, Week 4, Week 8, Week 12a functional test measuring clinical balance performance, and it has been shown to predict fall risk among elderly subjects (seconds)
Change from baseline in Range of motion score at every visitWeek 0, Week 2, Week 4, Week 8Compare flexion and extension angle using long arm goniometer between experimental and comparator group
Difference between the EuroQol Visual Analogue Scale (EQ-VAS) at each timepoint and baseline, respectivelyWeek 0, Week 2, Week 4, Week 8EQ-VAS uses a vertical 10cm line labeled at each end with scale anchors. EQ-VAS is used to indicate the patient's health state and patients are asked to mark a point that represents their health state between the anchors of 'worst health state' and 'best health state imaginable'. Scores are recorded in millimeters with a total range of 0-100 millimeters.
Cost per QALY(Quality Adjusted Life Years) gainedWeek 0, Week 4, Week 8, Week 12The quality of life estimation for QALY calculation will use the quality of life derived from EQ-5D as the main evaluation variable, and the calculation method is using Area under the curve method
Change from baseline in Timed Up and Go Test at every visitWeek 0, Week 2, Week 4, Week 8, Week 12a functional test evaluating the time to rise from a chair, walk 3 meters, turn around, walk back to the chair and sit down (abnormal cut-off value \>12 seconds).

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026