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To evaluate the efficacy of digital occlusal splint in the treatment of loose teeth in moderate/severe periodontitis

To evaluate the efficacy of digital occlusal splint in the treatment of loose teeth in moderate/severe periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124545
Enrollment
Unknown
Registered
2026-05-13
Start date
2026-05-15
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Moderate/severe periodontitis

Interventions

Control group:Initial periodontal treatment
Group OS2:Initial periodontal treatment and digital occlusal splint treatment
Group OS1:Initial periodontal treatment and vacuum diaphragm occlusal splint treatment were performed

Sponsors

The First Hospital of Nanchang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 30 - 70 years old; 2. The patient has at least one tooth that is loose, and at least one of the loose teeth has a degree of looseness ranging from grade II to grade III. The patient strongly requests to keep the affected tooth; 3. The patient has good compliance and attends regular follow-up visits.

Exclusion criteria

Exclusion criteria: 1. Patients with severe systemic diseases or whose systemic diseases are not under control (diabetes, hematological diseases, osteoporosis, rheumatoid arthritis, tumors), who cannot cooperate with the researchers; 2. Teeth with longitudinal cracks or root fractures; 3. Teeth sensitive to cold and hot stimuli; 4. Abutment teeth of fixed bridges and removable partial dentures; 5. Patients with temporomandibular joint disorders; 6. Patients with nocturnal bruxism habit; 7. Patients with malocclusion (bite) or overbite (bite), or patients undergoing orthodontic treatment; 8. Pregnant or post-pregnancy women; 9. Severe smokers, smoking >= 10 cigarettes/day; 10. Patients who cannot follow up as scheduled, have poor compliance, or have incomplete data.

Design outcomes

Primary

MeasureTime frame
Degree of loosening;The degree of tooth mobility;Degree of alveolar bone loss;Occlusal splint comfort were evaluated;Crown root ratio;Clinical periodontal attachment loss;Bleeding index;Positive rate of plaque;Occlusal discomfort;Probing depth of periodontal pockets,;

Countries

China

Contacts

Public ContactDeng Wei

The First Hospital of Nanchang

963964265@qq.com+86 791 8677 1017

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026