Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2023-01-01
2024-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Autologous Tooth Root+Vit.D3+Bone graft
Placement of bone graft and local administration of Vit.D3, and placement of autologous root slices
Autologous Tooth Root
An autologous Tooth Root is made from one's own tooth root and covered in an extraction socket where bone graft is placed.
Vit.D3
Local administration of Vit.D3, through the effect of Vit.D3 to explore whether it can help to accelerate the healing of tooth extraction cavity and the clinical effectiveness of bone regeneration.
bone graft
Selecting bone materials for alveolar ridge preservation according to treatment needs
Autologous Tooth Root+ Bone graft
Placement of bone graft without local administration of Vit.D3 and placement of autogenous root slices
Autologous Tooth Root
An autologous Tooth Root is made from one's own tooth root and covered in an extraction socket where bone graft is placed.
bone graft
Selecting bone materials for alveolar ridge preservation according to treatment needs
Bone graft
Only bone graft materials were placed, no local administration of Vit.D3, and no autologous root slices were placed
bone graft
Selecting bone materials for alveolar ridge preservation according to treatment needs
Natural healing
After the wound healed naturally, no bone graft material was filled, and Vit.D3 was not administered locally, and autologous tooth root slices were not placed.
No interventions assigned to this group
Interventions
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Autologous Tooth Root
An autologous Tooth Root is made from one's own tooth root and covered in an extraction socket where bone graft is placed.
Vit.D3
Local administration of Vit.D3, through the effect of Vit.D3 to explore whether it can help to accelerate the healing of tooth extraction cavity and the clinical effectiveness of bone regeneration.
bone graft
Selecting bone materials for alveolar ridge preservation according to treatment needs
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. The extraction socket is located in the anterior and posterior areas of the upper and lower jaws.
3. The intraoral extraction socket (bone defect) area will need to receive artificial dental implant treatment in the future.
4. The patient does not have systemic disease.
5. Patients who do not have systemic diseases (such as hypertension, diabetes, heart disease, osteoporosis, bone-related diseases, kidney diseases, thyroid and parathyroid diseases, etc.), and those who need to take preventive antibiotics before tooth extraction/surgery (artificial valve/stent, artificial joint).
Exclusion Criteria
2. Women who are pregnant or breastfeeding.
3. Exclude heavy smokers or betel nut chewers who smoke more than one pack of cigarettes per day.
4. The bone defect of the extraction socket is severe (especially if the vertical height of the buccal bone defect \[corono-apical\] exceeds 1/2), other bone regeneration surgery (GBR) is required, otherwise it is impossible to have sufficient alveolar bone height in the future and widths to provide artificial dental implants
5. The root of the tooth has been severely damaged, the root of the active periodontal ligament is lacking, and it is not suitable for autologous root sectioning, and the alveolar bone and apical defect after tooth extraction are severe (the apical lesion with a defect diameter of \>3mm in root apex X-ray examination) \[apical lesion\])
20 Years
70 Years
ALL
Yes
Sponsors
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Chang Gung Memorial Hospital
OTHER
Responsible Party
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Hsiang-Hsi Hong
Professor-level attending physician
Principal Investigators
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Hsiang H Hong
Role: PRINCIPAL_INVESTIGATOR
Chang Gung Memorial Hospital
Locations
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Chang Gung Memorial Hospital
Taoyuan District, , Taiwan
Countries
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Other Identifiers
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202002350A0
Identifier Type: -
Identifier Source: org_study_id
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