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Trial · NCT01770912

Registered outcomes15

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange From Pre-Treatment in TMJ Loading Pain Rating at 12 WeeksBaseline and 12 weeks post-treatmentTMJ loading pain is evaluated using ordinal scale ratings of 0-3 (none, mild, moderate, severe pain intensity).
SecondaryChange From Pre-Treatment in TMJ Loading Pain Rating at 2 WeeksBaseline and 2 weeks post-treatmentTMJ loading pain is evaluated using ordinal scale ratings of 0-3 (none, mild, moderate, severe pain intensity).
SecondaryChange From Pre-Treatment in TMJ Loading Pain Rating at 6 WeeksBaseline and 6 weeks post-treatmentTMJ loading pain is evaluated using ordinal scale ratings of 0-3 (none, mild, moderate, severe pain intensity).
SecondaryChange From Pre-Treatment in Mandibular Range of Motion Without Pain at 2 WeeksBaseline and 2 weeks post-treatment
Mandibular range of motion is measured in millimeters (mm) of vertical opening between the upper and lower central incisors plus vertical overlap of the incisors. These measures are made for jaw unassisted opening without pain, maximum unassisted opening and maximum assisted opening. Horizontal mandibular range of motion is measured in millimeters (mm) assessed for maximal right and left mandibular lateral movements and mandibular protrusion. A positive value represents an improvement (or larger range of motion) in mandibular opening/lateral movement.
SecondaryChange From Pre-Treatment in Mandibular Range of Motion at 6 WeeksBaseline and 6 weeks post-treatment
Mandibular range of motion is measured in millimeters (mm) of vertical opening between the upper and lower central incisors plus vertical overlap of the incisors. These measures are made for jaw unassisted opening without pain, maximum unassisted opening and maximum assisted opening. Horizontal mandibular range of motion is measured in millimeters (mm) assessed for maximal right and left mandibular lateral movements and mandibular protrusion. A positive value represents an improvement (or larger range of motion) in mandibular opening/lateral movement.
SecondaryChange From Pre-Treatment in Mandibular Range of Pain-Free Motion at 12 WeeksBaseline and 12 weeks post-treatment
Mandibular range of motion is measured in millimeters (mm) of vertical opening between the upper and lower central incisors plus vertical overlap of the incisors. These measures are made for jaw unassisted opening without pain, maximum unassisted opening and maximum assisted opening. Horizontal mandibular range of motion is measured in millimeters (mm) assessed for maximal right and left mandibular lateral movements and mandibular protrusion. A positive value represents an improvement (or larger range of motion) in mandibular opening/lateral movement.
SecondaryChange From Pre-Treatment Palpable Muscle Tenderness at 2 WeeksBaseline and 2 weeks post-treatment
Palpable muscle tenderness of masticatory muscles using ordinal ratings of 0-3 (none, mild, moderate, severe pain to palpation) are summed. A standardized muscle palpation pressure is used at specific locations on each side of the face for a total of 20 locations. The range of possible scores is 0-60. The rating of each muscle palpation site is added for a composite muscle tenderness score.
SecondaryChange From Pre-Treatment Palpable Muscle Tenderness at 6 WeeksBaseline and 6 weeks post-treatment
Palpable muscle tenderness of masticatory muscles using ordinal ratings of 0-3 (none, mild, moderate, severe pain to palpation) are summed. A standardized muscle palpation pressure is used at specific locations on each side of the face for a total of 20 locations. The range of possible scores is 0-60. The rating of each muscle palpation site is added for a composite muscle tenderness score.
SecondaryChange From Pre-Treatment Palpable Muscle Tenderness at 12 WeeksBaseline and 12 weeks post-treatment
Palpable muscle tenderness of masticatory muscles using ordinal ratings of 0-3 (none, mild, moderate, severe pain to palpation) are summed. A standardized muscle palpation pressure is used at specific locations on each side of the face for a total of 20 locations. The range of possible scores is 0-60. The rating of each muscle palpation site is added for a composite muscle tenderness score.
SecondaryNumber of Participants With Change From Pre-Treatment Joint Sounds in 2 WeeksBaseline and 2 weeks post-treatmentOpening and closing sounds (click, course crepitus, fine crepitus) detected by palpation on left, right or both sides of face.
SecondaryNumber of Participants With Change From Pre-Treatment Joint Sounds in 6 WeeksBaseline and 6 weeks post-treatmentOpening and closing sounds (click, course crepitus, fine crepitus) detected by palpation on left, right or both sides of face.
SecondaryNumber of Participants With Change From Pre-Treatment Joint Sounds in 12 WeeksBaseline and 12 weeks post-treatmentOpening and closing sounds (click, course crepitus, fine crepitus) detected by palpation on left, right or both sides of face.
SecondaryChange From Pre-Treatment Functional Pain (Chewing) at 2 WeeksBaseline and 2 weeks post-treatmentPain is assessed for average chewing pain intensity using a 100 mm visual analog scale with 0 representing "no pain" and 100 representing "the most intense chewing pain imaginable".
SecondaryChange From Pre-Treatment Functional Pain (Chewing) at 6 WeeksBaseline and 6 weeks post-treatmentPain is assessed for average chewing pain intensity using a 100 mm visual analog scale with 0 representing "no pain" and 100 representing "the most intense chewing pain imaginable".
SecondaryChange From Pre-Treatment Functional Pain (Chewing) at 12 WeeksBaseline and 12 weeks post-treatmentPain is assessed for average chewing pain intensity using a 100 mm visual analog scale with 0 representing "no pain" and 100 representing "the most intense chewing pain imaginable".

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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