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A prospective, randomized, controlled clinical study of periodontitis vertical increment with periodontal regeneration in labia (buccal) horizontal bone resorption with periodontal pocket

A prospective, randomized, controlled clinical study of periodontitis vertical increment with periodontal regeneration in labia (buccal) horizontal bone resorption with periodontal pocket

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057151
Enrollment
Unknown
Registered
2022-03-01
Start date
2022-07-06
Completion date
Unknown
Last updated
2023-10-03

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

Conditions

Periodontitis

Interventions

experimental group:periodontal regeneration
control group:periodontal flap surgery

Sponsors

Stomatological Hospital Affiliated to Nanjing University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were clinically diagnosed with chronic or invasive periodontitis according to the diagnostic criteria of the 1999 International Classification of Periodontitis; Patients were classified as stage III grade C according to the staging criteria of periodontitis in the 2018 New International Classification of periodontal Disease and peri-implant disease; 2. Aged 18-65 years, no gender limit; 3. Total oral plaque score (FMPS) and total oral bleeding score (FMBS) were less than 15% at baseline; 4. The lesions may involve single or multiple teeth, but the lesions of multiple teeth are not accompanied by root bifurcation lesions; 5. The lesion site requires surgical treatment and meets all the following conditions: (1) PD>=5mm at baseline; (2) After intraoperative debridement, the defect of the lesion site was mainly horizontal bone defect, and only one surface of the lip and buccal surface occurred, and the site could be maxillary or mandibular, and the depth was less than 2mm if there was vertical bone defect; (3) Keratinized gingiva with a width of >=2mm so that bone defects and implants can be completely covered; (4) Radiological examination of horizontal bone defect >=4mm; 6. Tooth loosening <= degree II; 7. Periodontal treatment with etiology (e.g., occlusal trauma) should be completed at least 3 months before screening; 8. The pulp of the test tooth is still viable or has received appropriate pulp treatment.

Exclusion criteria

Exclusion criteria: 1. The test tooth had a history of periodontal surgery; 2. Patients with systemic diseases affecting periodontal healing; 3. A variety of subjects that can lead to oral imaging artifacts, such as: the study tooth and its adjacent teeth are metal dentures, porcelain teeth; 4. Pregnancy or lactation; 5. Patients allergic to recycled materials; 6. Patients who have used drugs affecting periodontal conditions in the past 6 months; 7. Patients with smoking habit, >=10 cigarettes per day; 8. After non-surgical treatment, total mouth plaque score (FMPS) and total mouth bleeding score (FMBS)>=25%; 9. Patients with poor compliance.

Design outcomes

Primary

MeasureTime frame
clinical attachment level;

Secondary

MeasureTime frame
probing depth;gingival recession;bleeding on probing;

Countries

China

Contacts

Public ContactLi Houxuan

Stomatological Hospital Affiliated to Nanjing University School of Medicine

1809198399@qq.com+86 18795863036

Outcome results

None listed

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