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Clinical Trials/KCT0003192
KCT0003192Completed未知

Clinical research of effectiveness and economic feasibility of Chuna manual therapy for temporomandibular disorder: A multicenter randomized controlled trial

Kyung Hee University0 sites80 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
未知
Status
Completed
Enrollment
80
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

  1. At the primary end point (5 week), VAS for TMD pain improved significantly in both group. But there was no significant difference between 2 groups. By the RM ANOVA, there was no significant difference in the change of VAS over time between 2 groups. 2. NRS for pain, NRS for bothersomeness of the TMD, and BDI score improved significantly in both groups, but there was no significant difference between 2 groups. JFLS improved significantly only in the CMT group.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
19(Year) to 70(Year) (—)
Sex
All

Inclusion Criteria

  • •1) Temporomandibular joint pain on one or both sides
  • •2) Temporomandibular joint pain intensity NRS(Numeral Rating Scale) = 4
  • •3) sustained temporomandibular joint pain for more than 3 months
  • •4) Patients diagnosed with myofascial temporomandibular joint disorders(Axis I: Group 1) in the RDC/TMD diagnostic criteria
  • •* RDC/TMD(Research Diagnostic Criteria for temporomandibular joint disorders)
  • •5) Informed consent for study participation
  • •6) Men or women aged between 19 and 70 years

Exclusion Criteria

  • •1) Temporomandibular Joint pain induced by traffic accident or traumatic injury
  • •2) excluded in myofascial temporomandibular joint disorders(Axis I: Group 1) based on the RDC/TMD diagnostic criteria
  • •* RDC/TMD(Research Diagnostic Criteria for Temporomandibular Disorders)
  • •3) paticipants after surgery with temporomandibular joint disorders
  • •4) other diseases (e.g., rheumatoid arthritis, tumor, stroke and myocardial infarction) that may interfere with the interpretation of the results.
  • •5) Treatment within the previous 1 week (NSAIDs, steroid, herbal drug, acupuncture, etc.)
  • •6) participants who recieved Chuna manual therapy within the previous 2 week
  • •7) Women with (suspected) pregnancy or breast-feeding
  • •8) Participation in another clinical study within the previous 1 month
  • •9) Difculty in communicating with the investigators

Investigators

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