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Conventional, Additive and Subtractive Occlusal Splints for TMDs

NCT07371078 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2026-01-27

No results posted yet for this study

Summary

This study is aiming to clinically compare between occlusal splints produced by conventional, subtractive and additive techniques in regard to patient satisfaction.

Conditions

  • TMD
  • Disc Displacement

Interventions

DEVICE

Conventional Stabilizing Splint

Manual Manufacturing

DEVICE

Milled Stabilizing Splint

Subtractive Manufacturing

DEVICE

3D Printed Stabilizing Splint

Additive Manufacturing

Sponsors & Collaborators

  • Mansoura University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-01
Primary Completion
2025-09-01
Completion
2025-12-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07371078 on ClinicalTrials.gov