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NCT04524806

Influence of Stabilization Splint Thickness on The Temporomandibular Disorders

Completed NA Last updated 24 August 2020
What this trial tests

NA trial testing stabilization splint in Temporomandibular Disorder in 104 participants. Completed in 30 January 2015.

Timeline
1 July 2013
Primary endpoint
1 January 2014
30 January 2015

Quick facts

Lead sponsorIstanbul Medipol University Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment104
Start date1 July 2013
Primary completion1 January 2014
Estimated completion30 January 2015

Drugs / interventions tested

Conditions studied

Sponsor

Istanbul Medipol University Hospital

Who can join

Adults 18 to 65, any sex, with Temporomandibular Disorder or Temporomandibular Joint Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is assessing the effect of the stabilization splint (SS) thickness on the temporomandibular disorder's and their symptoms; such as muscle or temporomandibular joint (TMJ) pain, TMJ sounds, and limitation of mouth opening.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of stabilization splint

Trials testing the same drug.

Other recruiting trials for Temporomandibular Disorder

Currently open trials in the same condition.

Other Istanbul Medipol University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04524806.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing