Skip to content

The effect of splint and electrical stimulating on temporomandibular joint disorders

Comparing the treatment efficacy of splint and electrical stimulating on temporomandibular joint disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016110730761N1
Enrollment
40
Registered
2016-12-15
Start date
2016-09-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Temporomandibular joint disorders. Temporomandibular joint disorders

Interventions

Intervention 1: Splint group: Using splint for 8 weeks
in the first 6 weeks it will be used 24 hours a day and from the 6th week till the end of the 8th week its usage will be reduced so at the end of 8th week it will be used only while sleeping. Interven
each session will last 30 minutes with a frequency of 80 Hz.
Treatment - Other
Splint group: Using splint for 8 weeks
in the first 6 weeks it will be used 24 hours a day and from the 6th week till the end of the 8th week its usage will be reduced so at the end of 8th week it will be used only while sleeping
Electrical stimulation group: the patients will receive 10 sessions of treatment through stimulation of the skin of the temporomandibular joint area
each session will last 30 minutes with a frequency of 80 Hz

Sponsors

Vice chancellor for research, Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age of 16-45 years; having normal teeth except the third molar tooth and Angle Class I occlusion and having occlusal interferences. Exclusion criteria: having systemic disease; organic disorders of temporomandibular joint; using antipsychotic drugs within the last two weeks; history of orthodontic treatment and having any prosthesis.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mean pain score. Timepoint: at the end of 8th week in the splint group and at the end of 10th session in the electrical stimulation group. Method of measurement: Using Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMostafa Ghayoor

Zahedan University of Medical Sciences

s-risbaf@zaums.ac.irmostafa7203603@yahoo.com+98 54 3329 5715

Outcome results

None listed

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