- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06141239
2D/3D Imaging to Analyze the Regeneration Rate of Autologous Bone
Using 2D/3D Imaging to Analyze the Regeneration Rate of Autologous Bone During Alveolar Bone Preservation Surgery Using Periodontal Valves to Completely Cover Autologous Tooth Roots, Bone Substitutes, and Vitamin D3 Treatment
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Wen H Chi
- Phone Number: +886983999157
- Email: news760730@gmail.com
Study Contact Backup
- Name: Hsiang Hsi Hong
- Phone Number: +886975365989
- Email: f1214@adm.cgmh.org.tw
Study Locations
-
-
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Taoyuan, Taiwan
- Recruiting
- Chang Gung Memorial Hospital
-
Contact:
- Hsi H Hong
- Phone Number: 0975365989
- Email: f1214@adm.ocgmh.org.tw
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Willing to sign written subject consent
- The tooth extraction socket is located in the anterior and posterior areas of the upper and lower jaws.
- The area of the extraction socket (bone defect) in the mouth will need to be treated with artificial dental implants in the future.
- The patient does not have systemic diseases (such as patients with hypertension, osteoporosis, bone-related diseases, kidney disease, thyroid and parathyroid diseases, etc.).
Exclusion Criteria:
- Patients with potentially weakened healing abilities such as cancer, diabetes, bone infection, tuberculosis, anemia due to heme abnormalities or congenital immune deficiency, cellulitis, acute periodontal cyst, severe cusp disease (cyst size) >2mm2) or patients with dental and jaw lesions.
- Women who are pregnant or breastfeeding.
- Exclude heavy smokers or betel nut chewers who smoke more than one pack of cigarettes per day.
- The bone defect in the extraction socket is severe and requires other bone regeneration surgeries (GBR), otherwise it will not be possible to have enough volume to provide artificial dental implants in the future.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: primary closure +Collagen plug +Bone graft
Placement of bone graft and collagen plug
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|
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Experimental: primary closure + Collagen plug +Bone graft +Vit.D3
Placement of bone graft, collagen plug and local administration of Vit.D3
|
Selecting bone materials for alveolar ridge preservation according to treatment needs
Other Names:
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
Other Names:
|
|
Experimental: primary closure +Collagen plug+Bone graft+Autologous Tooth Root
Placement of bone graft, collagen plug and placement of autologous root slices
|
An autologous Tooth Root is made from one's own tooth root and covered in an extraction socket where bone graft is placed.
Selecting bone materials for alveolar ridge preservation according to treatment needs
Other Names:
|
|
Experimental: primary closure +Collagen plug+Bone graft+Autologous Tooth Root+Vit.D3
Placement of bone graft, collagen plug and local administration of Vit.D3, and placement of autologous root slices
|
An autologous Tooth Root is made from one's own tooth root and covered in an extraction socket where bone graft is placed.
Selecting bone materials for alveolar ridge preservation according to treatment needs
Other Names:
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
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
3D computed tomography data
Time Frame: At the 0th week and 12th~16th week of the experiment
|
This experiment mainly used the relative position of the extraction socket and the adjacent tooth CEJ in CT images for height positioning and correction, and measured and compared the changes of the width and height of the bone ridge - Page 3 of 5 - and the shape and volume during the treatment. The Hu value of the adjacent dentin of the secondary CT was used as the standard and correction to measure and compare the change of the Hu value of the extraction socket during the treatment |
At the 0th week and 12th~16th week of the experiment
|
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periapical X-ray
Time Frame: 16 weeks after tooth extraction (before dental implants or other treatments)
|
Take X-rays 16 weeks after tooth extraction (before dental implants or other treatments), record the width and height of the alveolar bone, and compare whether there is any difference in pixel values between the extraction socket and the adjacent non-extraction area, by calculating the number of pixels The difference in gray scale depth (i.e.
density) of the image is determined by size to infer the formation of autogenous bone.
|
16 weeks after tooth extraction (before dental implants or other treatments)
|
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Intraoral scanner measurement data
Time Frame: At the 0th week and 12th~16th week of the experiment
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Follow-up observation and measurement: Intraoral photography scans were performed 0 weeks after tooth extraction/alveolar ridge preservation to record the appearance of soft tissues, including soft tissue thickness, buccal keratinized gingival width and thickness, and 16 weeks after surgery before dental implant surgery or other treatments.
A second intraoral photography scan was performed to record the soft tissue condition again and compare the soft tissue wound healing evolution of the two tooth extraction cavities.
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At the 0th week and 12th~16th week of the experiment
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RFA measures implant stability (ISQ)
Time Frame: At the 16th~24th week of the experiment
|
The implant stability was measured twice during the dental implant surgery at 16 to 24 weeks.
The ISQ value of the 3.3mm diameter implant measured by Osstell Mentor was used as the standard ISQ value for correction.
After the 3.3mm implant was removed, the matching funds would not be Then use a 3.3mm implant, and then measure the ISQ value of the implant (diameter 4.1 or 4.8mm) as the actual ISQ value of the initial stability of the implant.
The implant repair will be made 3-4 months after the operation.
Before implantation), measure the ISQ value of the second-stage stability of the implant to compare and analyze the changes in ISQ value of different implant groups and/or time points.
Each subject followed this procedure.
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At the 16th~24th week of the experiment
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202102214A0
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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