Investigation of patients with craniomandibular dysfunction before and after physiotherapy and splint therapy.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00030298

Enrollment

Registered

2023-01-16

Start date

2019-09-29

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

temporomandibular dysfunction (TMD) K07.6

Interventions

Group 1: In this study, the change in spinal and body posture of TMD patients before, during and after treatment with manual and splint therapy is evaluated in three dimensions using raster stereograp

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: • Age of majority • Positive "CMD screening test" according to Jakstat and Ahlers

Exclusion criteria

Exclusion criteria: • Minor • Previously known or no definite TMD diagnosis • Previously received TMD treatments (medications, massages, exercises, splint, etc.) • Surgery on the temporomandibular joint and surrounding structures

Design outcomes

Primary

Measure	Time frame
CMD group: Completion of follow-up of subjects after completion of remedy prescription and splint therapy. Control group: completion of follow-up of subjects after 6 months. All subjects are examined raster stereographically and by intraoral scan at different time points and the changes over time are analyzed. Thus, the CMD patients receive five measurement time points within half a year and the control group receives two measurement time points within this period.	—

Measure

Time frame

CMD group: Completion of follow-up of subjects after completion of remedy prescription and splint therapy. Control group: completion of follow-up of subjects after 6 months. All subjects are examined raster stereographically and by intraoral scan at different time points and the changes over time are analyzed. Thus, the CMD patients receive five measurement time points within half a year and the control group receives two measurement time points within this period.

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Countries

Germany

Contacts

Public ContactRagai Matta

Universitätsklinikum Erlangen, Zahnklinik 2, Zahnärztliche Prothetik

ragai.matta@uk-erlangen.de09131/85-33604

Outcome results

None listed

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