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NCT04455672

A Comparative Study Using Two 3D Printed Occlusal Splints for Patients With Tempromandibular Disorder

Status unknown NA Last updated 2 July 2020
What this trial tests

NA trial testing splints in Temporomandibular Disorder in 24 participants. Status unknown.

Timeline
1 July 2020
Primary endpoint
26 July 2021
26 September 2021

Quick facts

Lead sponsorCairo University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment24
Start date1 July 2020
Primary completion26 July 2021
Estimated completion26 September 2021

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 20 to 50, male only, with Temporomandibular Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

• to compare the relief of pain for patients with anterior disc displacement with reduction between two groups; in the first group a digitally formed stabilizing splint followed by an anterior repositioning splint (ARS) and the second group a digitally fabricated (ARS) splints followed by a stabilizing splints

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. 3D-Printed anterior repositioning splint versus stabilization splint for patients with anterior disc displacement with reduction: A randomized cross-over clinical trial.
    Tahoon MMS, Abdelnabi NM, Elsisy AME, Moussa ARA, et al · · 2025 · cited 1× · PMID 40213888 · DOI 10.4103/jips.jips_8_25

Verify or expand the search:

Other recruiting trials for Temporomandibular Disorder

Currently open trials in the same condition.

Other Cairo University 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/NCT04455672.

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