Role of psychosocial factors in the etiology of bruxism.
Daniele Manfredini, Frank Lobbezoo
https://pubmed.ncbi.nlm.nih.gov/19492540Actively Recruiting
Led by University of Baghdad · Updated on 2025-08-07
60
Participants Needed
1
Research Sites
4 weeks
Total Duration
Researchers are evaluating the clinical effectiveness of chlorzoxazone compared to orphenadrine citrate for relieving orofacial pain in people who grind their teeth (bruxism). The study is a randomized clinical trial involving 60 patients over 15 years old who have orofacial and temporomandibular pain but no chronic systemic illnesses. The goal is to assess how well each drug reduces pain severity and improves temporomandibular joint function. Participants are randomly assigned to one of two groups: one group receives chlorzoxazone twice daily for two weeks, while the other group receives orphenadrine citrate on the same schedule. Both treatments are taken orally. Pain severity is measured using the Visual Analogue Scale (VAS) at the start, after 7 days, and after 14 days. A temporomandibular joint evaluation form is also used before and after treatment to assess joint parameters. During the study, participants will undergo pain assessments and joint evaluations at specified intervals. Researchers will monitor changes in orofacial pain scores from baseline to the end of treatment at two weeks. Statistical analysis will be conducted to compare the effects of the two drugs. The study is sponsored by the University of Baghdad and aims to provide detailed information on managing bruxism-related pain.
CONDITIONS
Effectiveness of Chlorzoxazone Versus Orphenadrine Citrate in Alleviating Bruxism Pain
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 2 weeks
Participants receive either Chlorzoxazone or Orphenadrine Citrate twice daily to alleviate bruxism-related orofacial pain.
Twice daily dosing for 2 weeks
Total: 1 location
1
College of Dentistry
Baghdad, Iraq
Actively Recruiting
N
Noor R. Al-Hasani, PhD
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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