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Management of Postoperative Pain Following Total Knee Arthroplasty by Using Acupuncture-moxibustion Therapy

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01047384
Enrollment
100
Registered
2010-01-12
Start date
2010-01-31
Completion date
Unknown
Last updated
2014-05-21

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

Conditions

Osteoarthritis, Knee

Brief summary

Orthopedic surgery is reportedly among the most painful surgical procedures. Surgical damage following major orthopedic surgery often involves a large, deep incision with considerable tissue dissection and muscle, bone, and vascular exposure. Post-operative pain after such surgery is exacerbated on movement or by reflex spasms of the muscles, which may delay mobilization, reduce satisfaction, prolong hospitalization, and possibly increase medical costs. We design a prospective randomized study for postoperative pain control following total knee arthroplasty.

Interventions

PROCEDUREacupuncture-moxibustion therapy

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* diagnosed for surgery of osteoarthritis of knee * ability to tolerate surgery under general anesthesia.

Exclusion criteria

* refusal or the lack of mental ability to provide informed consent * neuropathic pain or sensory disorders in the leg requiring surgery * previous surgery of the knee joint * coagulation abnormalities * chronic opioid users * known history of intolerance to acupuncture-moxibustion therapy

Design outcomes

Primary

MeasureTime frame
Pain VAS scorepre-operaton, immediately post operation, postop 6hrs, postop 12hrs, postop 18hrs, postop 24hrs, post op 48hrs, postop 72hrs

Secondary

MeasureTime frame
Functional score: SF-36Pre-operation, immediately post-operation, postop 6 weeks, postop 12 weeks

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026