Osteoarthritis
Conditions
Keywords
Osteoarthritis, Knee, Fumigation, Acupuncture
Brief summary
To evaluate the effect of fumigation in conjunction with acupuncture for knee osteoarthritis, participators were collected from acupuncture and Chinese traumatology clinic at Linsen Chinese Medicine and Kunming Branch, Taipei City Hospital. Participators were randomized into 3 groups, one for acupuncture with fumigation, one for acupuncture with diluted fumigation, one for acupuncture only.
Detailed description
Patient population. Between June 2015 and November 2017, research subjects were recruited via poster display and clinician referral, to participate in a three-armed, randomized, controlled trial to be conducted in the Traumatology Department Linsen Chinese Medicine and Kunming Branch, Taipei City Hospital.
Interventions
OTHERFumigation
use Fumigation to increase the improvement of osteoarthritis of knee
OTHERAcupuncture
Acupuncture
Sponsors
Taipei City Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Osteoarthritis of knee diagnosed by X-ray films * According Ahlbäck System, more than stage1 * The Visual Analogue Scale of pain over 20mm in 100mm
Exclusion criteria
* The Visual Analogue Scale of pain less than 20mm in 100mm * Received injection or scope treatment over knees * Received more than 3 times of operation * With severe inflammation (including fever, fluid, pus, gout, Rheumatic arthritis, etc.) * With sever systemic diseases (including metastatic cancer, coronary artery disease, lung disease, etc.) * With history of skin problem after other thermal treatment * Under other experiments * Women with pregnant, breastfeeding or prepare for pregnancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Visual Analogue Scale of pain | This numeric measure is assed and recorded pre and post intervention at each of the study protocols bi-weekly interventions over (4) weeks, for a maximum of (8) sessions and a total of (16) measurements per individual patient. | This scale is used to asses change in pain intensity between pre and post intervention measures and change against established baseline measures. Patients are asked to rate their pain by choosing a number along a horizontal line of fixed length (100mm). The number scale ranges from 0-10, with 0 representing 'no pain' and 10 being 'worst pain possible'. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Questionnaire | This questionnaire is administered and recorded after patients have been enrolled in the trial and prior to their first intervention to establish a baseline. At the completion of the protocol's full course of treatment, bi-weekly treatment over (4) weeks | Record Questionnaire before the study starting and after study finished |
Countries
Taiwan
Outcome results
None listed