Efficacy and Safety of JHG002 for Chronic Temporomandibular Joint Dysfunction: A Multicenter Randomized Controlled Trial

Jaseng Medical Foundation

Status: Completed

Conditions: Temporomandibular Disorder

Treatments: Other: hominis placental pharmacopuncture

Study type: Interventional

Funder types: Other

Identifiers

NCT04087005

JS-CT-2017-04

Details and patient eligibility

About

This study is a 2-arm parallel, assessor blinded, multi-centre, randomised controlled trial.

Full description

From 2 hospitals of Korean medicine, we will enrol 82 chronic TMD patients in Axis 1, Group Ⅰ according to RDC/TMD diagnostic criteria, and randomly allocate 41 patients each to an HPP group and a physical therapy (PT) group. Treatment will be administered in 10 rounds, after which there will be 4 follow-up visits (6, 9, 13, and 25 weeks from baseline). The primary end point is 6 weeks after baseline, and the primary outcome is the difference in Visual analogue scale (VAS) score for temporomandibular pain between baseline and Week 6. Secondary outcomes will be Numeric rating scale (NRS) scores for temporomandibular pain and discomfort, temporomandibular joint range of motion, Korean version of Beck's Depression Index-Ⅱ(K-BDI-II), Jaw Functional Limitation Scale (JFLS), Patien Global Impression of Change(PGIC), and quality of life. Using data on adverse events and cost-effectiveness in the two groups, we will perform a safety assessment and a cost-effectiveness analysis (economic assessment).

Enrollment: 82 patients

Sex: All

Ages: 19 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patients with unilateral or bilateral TMJ pain
2. Patients with VAS≥40mm for the area showing TMJ pain (for patients with bilateral pain, the side with worse pain)
3. Patients complaining of persistent of sporadic TMJ pain for at least 3 months
4. Patients diagnosed as myofascial TMD (Axis I: Group 1) based on the RDC/TMD diagnostic criteria[5]
5. Patients aged 19-70 years on the date they sign the consent form
6. Patients who provide consent to participate in the trial and return the informed consent form

Exclusion criteria

1. Patients whose current pain episode developed or worsened because of a road traffic accident or traumatic injury
2. Patients diagnosed in Group 2 or 3 of Axis I based on the RDC/TMD diagnostic criteria
3. Patients who have undergone surgery related to the TMJ
4. Patients with other chronic disease that could interfere with interpretation of the treatment effects or outcomes (e.g., rheumatoid arthritis, neoplastic disease, stroke, or myocardial infarction)
5. Patients currently taking steroids, immunosuppressants, psychiatric drugs, or other drugs that could affect the study results
6. Patients who have received HPP within the last month, or who have taken drugs that could affect pain, such as NSAIDs, within the last week
7. Pregnant or breastfeeding women
8. Patients who have finished participation in another clinical trial within the last month, who participated in another trial within 6 months of selection, or who are planning to participate in another clinical trial during the follow-up period
9. Patients with a history of hypersensitivity after HPP
10. Diabetic patients with uncontrolled blood glucose (fasting blood glucose ≥180mg/dl)
11. Patients with AST (GOT) or ALT (GPT) at least 2 times the normal range at the testing centre
12. Patients with creatinine at least 2 times the normal range at the testing centre
13. Patients suspected to have organic disease
14. Patients with cardiac, hepatic, renal, or other serious complications
15. Patients with psychogenic disease
16. Patients who are unable to receive pharmacopuncture due to e.g., inflammation or a wound at the relevant acupoints
17. Other patients whose participation in the trial is judged by a researcher to be problematic

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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82 participants in 2 patient groups

Hominis placental pharmacopuncture

Experimental group

Description:

The Hominis placental pharmacopuncture group will receive 10 sessions of Hominis placental pharmacopuncture at 2 sessions/week for 5 weeks. A trained doctor of Korean medicine with at least 2 years clinical experience will administer JHG002 pharmacopuncture with a disposable syringe (0.5ml) directly into the designated sites, using a standardized method.

Treatment:

Other: hominis placental pharmacopuncture

Transcutaneous electrical nerve stimulation

Active Comparator group

Description:

The control group will receive 2 sessions/week of TENS for 5 weeks. A high-frequency, low-intensity stimulus of 50-100Hz and up to 15mA will be used, such that the patients feel a current but do not feel pain. At each treatment visit, a physiotherapist will administer the treatment to the bilateral temporomandibular joint for 15 minutes. Both centres will use the same TENS device-a BioTron-DX (D.M.C, Osan, South Korea).

Treatment:

Other: hominis placental pharmacopuncture