Evaluation of the efficacy and quality of life in patients with temporomandibular joint disorders treated with Kovacs digital occlusal splint

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300076518

Enrollment

Unknown

Registered

2023-10-11

Start date

2022-09-01

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Temporomandibular joint diseases

Interventions

Kovacs digital occlusal splint group:Treatment of temporomandibular joint diseases using the kovacs digital occlusal splint

Eligibility

Sex/Gender

All

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) anterior disc displacement with or without reduction (ADDwR or ADDwoR) confirmed by magnetic resonance imaging, (2) age =18 years, (3) no history of any treatment for TMD, and (4) at least having a 3-month follow-up record.

Exclusion criteria

Exclusion criteria: (1) long-term chronic diseases, such as diabetes and immune diseases, which may affect the QoL of the patients; (2) cognitive dysfunction; and (3) incomplete follow-up data.

Design outcomes

Primary

Measure	Time frame
Pain score;Joint noise;Quality of life level;	—

Countries

China

Contacts

Public ContactXiao Jin

Stomatology Hospital Affiliated to Wenzhou Medical University

xiaojdoctor@sohu.com+86 134 5484 6979

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026