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Trial of antiinflammatory agent effect for TMD(myalgia of the masticatory muscle and arthralgia of the temporomandibular joint).

Trial of antiinflammatory agent effect for TMD(myalgia of the masticatory muscle and arthralgia of the temporomandibular joint). - Trial of antiinflammatory agent effect for TMD(myalgia of the masticatory muscle and arthralgia of the temporomandibular joint).

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029972
Enrollment
100
Registered
2017-11-14
Start date
2017-07-03
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Temporomandibular disorders

Interventions

Celecoxib group(fifty people administerd Celecoxib 100mg 2T/day for 14day) Loxoprofen group(fifty people administerd Loxoprofen 60mg 3T/day and Mazuren Combination Tablete 1.0es 3T/day for 14day)

Sponsors

Saga University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patient diagnosed TMD 2)Patient aged from 15 to 70years old 3)Patient agreed this trial in writing

Exclusion criteria

Exclusion criteria: 1)Patient suffer from malignant tumor 2)Patient have medical history of hypersensivity to Sulfonamide and prescription drug 3)Patient have medical history of aspirin asthma 4)Patient suffer from peptic ulcer 5)Patient suffer from severe hepatopathy 6)Patient suffer from severe nephropathy 7)Patient suffer from blood disease 8)Patient suffer from cardiac function disturbance 9)Perioperative patient of coronary artery bypass operation 10)Patient take aspirin to prevent for cardiovascular disease 11)Patient have medical history of cardiovascular disease and cerebrovascular disorder 12)Last pregnanncy patient 13)Patient taken other anti-inframmatory analgesic 14)Patient who is judged inappropriate by doctor

Design outcomes

Primary

MeasureTime frame
Pain and Maximum mouth opening (with or without pain) assessed as of firstexamination,1week and 2week after administration

Countries

Japan

Contacts

Public ContactKeisuke Mori

Saga University Hospital Department of oral and maxillofacial surgery

e6417@cc.saga-u.ac.jp0952-34-2397

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026