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Canceled by the investigator. A randomized controlled clinical trial on the use of different bone graft materials combined with extraction and alveolar ridge preservation in patients with severe periodontitis

Clinical application of different bone graft materials combined with extraction and alveolar ridge preservation in patients with severe periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074812
Enrollment
Unknown
Registered
2023-08-16
Start date
2023-09-01
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

severe periodontitis

Interventions

control group:minimally invasive tooth extraction
test group 1:Minimally invasive tooth extraction, implanting bio-oss into the extraction socket, and applying Bio Gide absorbable membrane covering bone graft materials and defect areas. Cover the sof
test group 2:Minimally invasive tooth extraction with Bio-Oss Collagen implanted in the extraction socket, Bio-Gide absorbable membrane covering bone graft materials and defect areas. Cover the soft t
test group 3:Minimally invasive tooth extraction with REBONE bone meal implanted in the extraction socket, Bio-Gide absorbable membrane covering bone graft materials and defect areas. Cover the soft t
test group 4:Minimally invasive tooth extraction with OSTEO GRART bone meal implanted in the extraction socket, Bio-Gide absorbable membrane covering bone graft materials and defect areas. Cover the s

Sponsors

Peking University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with hypertension and diabetes who are generally healthy or well controlled; 2. Can maintain good oral hygiene and good compliance; 3. There are teeth in the mouth that need to be extracted due to severe periodontal disease: PD > 6mm, AL >= 5mm, imaging examination shows alveolar bone resorption exceeding 1/2 or more of the root length, molar with furcation involvement, and tooth looseness > II°; 4. There is bone defect in the affected alveolar fossa, with at least two bone walls with a height of >= 3mm (buccal,lingual, mesial and distal bone walls); 5. At least one adjacent tooth exists.

Exclusion criteria

Exclusion criteria: 1. Patients aged = 10 cigarettes per day; 3. Pregnant or lactating women; 4. History of head and neck radiation therapy; 5. Long term use of non-steroidal anti-inflammatory drugs, corticosteroids, tetracyclines, bisphosphonates, or other drugs that affect bone regeneration; 6. The dentition is significantly crowded, ectopic, and twisted; 7. There is acute infection of the affected tooth; 8. Gingival hyperplasia.

Design outcomes

Primary

MeasureTime frame
changes in width of buccal keratinized tissue and soft tissue thickness;changes in three-dimensional morphology of soft and hard tissue contours;changes in height and width of alveolar bone;changes in soft tissue morphology;histology of bone blocks;periodontal clinical indicators;

Secondary

MeasureTime frame
postoperative reactions;bone grafting during implantation surgery;Health Economics;surgical time;

Countries

China

Contacts

Public ContactHu Wenjie

Peking University School and Hospital of Stomatology

huwenjie@pkuss.bjmu.edu.cn+86 139 1107 0329

Outcome results

None listed

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