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clinical study of warming needle moxibustion combined with joint mobilization on temporomandibular disorders

clinical study of warming needle moxibustion combined with joint mobilization on temporomandibular disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005896
Enrollment
Unknown
Registered
2022-04-23
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

temporomandibular disorders

Interventions

joint mobilization group(control group):joint mobilization
warming needle moxibustion combined with joint mobilization group(treatment group):warming needle moxibustion combined with joint mobilization

Sponsors

Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Diagnosed with temporomandibular disorders according to Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) (2)maximum mouth opening (MMO) < 40mm and visual analogue scale (VAS) score = 2 (3)aged 18-70 and can cooperate with treatment and examination (4)First onset and have not received any therapy for six months (5)Voluntarily participate in this study, insist on completing the entire treatment process, and sign the informed consent

Exclusion criteria

Exclusion criteria: (1)A history of temporomandibular joint trauma or surgery; (2)Temporomandibular tumors, autoimmune bone and joint system diseases; (3)Combined with serious underlying diseases (heart, lung, liver, kidney dysfunction), or other serious life-threatening diseases; (4)taking certain drugs (antidepressant, antischizophrenia, non-steroidal anti-inflammatory medications and muscle relaxants); (5)Special populations (pregnant women, patients with coagulopathies); (6)Have other diseases and factors that are not compatible with treatment.

Design outcomes

Primary

MeasureTime frame
Clinical efficacy rate;

Secondary

MeasureTime frame
mandibular function impairment questionnaire,MFIQ;OHIP-14;Visual Analogue Scale,VAS;Maximum active mouth opening,MMO;craniomandibular index,CMI;

Countries

China

Contacts

Public ContactYu Jing
zegnajing@163.com18757576550

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026