ClinicalTrials.Veeva

Menu

Effect of Laser Therapy Versus Anterior Re-positioning Splint in the Treatment of Disc Displacement With Reduction

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Temporomandibular Joint Disorders

Treatments

Device: inactive Laser therapy
Device: anterior re-positioning splint
Device: Laser therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT03576079
CEBD-CU-2015-02-25

Details and patient eligibility

About

comparing the effects of Laser therapy with anterior re-positioning splint and a placebo group on clinical signs and symptoms of temporo-mandibular dis-function and assessing articular disc morphology and configuration with magnetic resonance imaging.

Full description

to compare the clinical effects of Laser therapy as assessed with research diagnostic criteria of temporo-mandibular disorders to a group that received anterior re-positioning splint therapy and a control group that received placebo Laser. Diagnosis for disc displacement with reduction was performed with magnetic resonance imaging before treatment. assessment of the clinical and MRI findings was again performed after a 3 months observation period.

Enrollment

30 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Patients having TMD in the form of disc displacement with reduction as verified from signs and symptoms during clinical examination and confirmed from the MRI.
  2. Good general health: The patient must be medically free from any systemic disease or health problems.
  3. Adult patients 18 years old and above.
  4. No previous orthodontic treatment.
  5. No previous TMJ treatment or surgery.

Exclusion criteria

  1. Patients with multiple missing posterior teeth.
  2. Muscle pain due to systemic disease.
  3. Dental related pain.
  4. Congenital abnormality, neoplasia or acute trauma.
  5. Previous TMJ treatment or surgery.
  6. Any medical condition that prohibits MRI acquisition.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 3 patient groups, including a placebo group

Laser therapy
Experimental group
Description:
12 laser sessions over 3 months
Treatment:
Device: Laser therapy
anterior re-positioning splint therapy
Active Comparator group
Description:
anterior re-positioning splint worn for 8 hours during night time for 3 months
Treatment:
Device: anterior re-positioning splint
inactive laser therapy
Placebo Comparator group
Description:
placebo laser for 12 sessions over 3 months
Treatment:
Device: inactive Laser therapy

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems