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Application of modified subgingival suspension suture

Application of modified subgingival suspension suture

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057518
Enrollment
Unknown
Registered
2022-03-14
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Periodontitis

Interventions

Experimental group:modified suspension suture
Control group:sling suture

Sponsors

Hospital of Stomatology Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Cone Beam Computed Tomography (CBCT) examination showed that labial alveolar bone was thin, or bone window and bone cracking were found; 2. No systemic disease; 3. No active periodontitis, PD depth <= 1mm; 4. No abnormal root, periapical periodontitis or malformed root; 5. No smoking history.

Exclusion criteria

Exclusion criteria: 1. The keratinized gingival width is less than 2mm; 2. Abnormal membrane gingival; 3. Patients with poor compliance, lost follow-up or interruption of treatment.

Design outcomes

Primary

MeasureTime frame
Alveolar bone increment;—

Countries

China

Contacts

Public ContactYang Dong

Wuhan University

yangdong9876@126.com+86 18571712883

Outcome results

None listed

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