Randomised clinical trial in subjects with temporomandibular dysfunction treated with Michigan Splint versus CAD/CAM Splint

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00004275

Enrollment

Registered

2012-08-09

Start date

2012-07-24

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

K07.6 F45.8

Interventions

Group 1: The control group is going to be treated with conventional manualy manufactured Michigan Splint Group 2: The treatment group is going to be treated with CAD/CAM Michigan Splint.

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Temporomandibular dysfunction

Exclusion criteria

Exclusion criteria: -Subjects younger than 20 years and older than 60 years-old. -Subjects having at the moment another disease that is not the TMD and that causes pain ( for instance, sinusitis or rheumatism). -Subjects with Orthodontics or Functional Maxillary Orthopedics or splint usage. -Subjects with craniofacial trauma in the last 6 months. -Subjects with muscle relaxant usage.

Design outcomes

Primary

Measure	Time frame
The primary outcome is the pain reduction measurement by numerical scale. The measurement is going to be made befor the intervention and than monthly during 9 months.	—

Secondary

Measure	Time frame
The secundary outcome is the change in mandibular movement that is going to be eletronically measured. The measurement is going to be made before the intervention and than in 3 and 6 months.	—

Countries

Germany

Contacts

Public ContactSandra Hüning

Poliklinik für Zahnärztliche Prothetik LMU München

Sandra.Huening@med.uni-muenchen.de04989 17699307145

Outcome results

None listed

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