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Autologous Tooth Root in Ridge Preservation

Chang Gung Medical Foundation logo

Chang Gung Medical Foundation

Status

Completed

Conditions

Alveolar Ridge Preservation

Treatments

Other: bone graft
Drug: Vit.D3
Procedure: Autologous Tooth Root

Study type

Interventional

Funder types

Other

Identifiers

NCT05601531
202002350A0

Details and patient eligibility

About

Use your extracted teeth for routine dental care to make an autologous root slice, cover it in your extraction cavity, and give you Vit.D3 locally with the bone material you use. The difference from traditional therapy is autologous Local use of tooth root slices and Vit.D3, bone materials and Vit.D3 are already qualified drugs on the market, but there is no precedent for making slices from autologous tooth roots, which will be a new medical technology that has not been used before test.

Full description

The anatomy of the alveolar bone around the teeth can be altered by tooth extraction. Bone ridge preservation can preserve/improve the quality and quantity of alveolar bone for future implants or dentures to promote predictable function and esthetics; in addition, extraction cavity closure can be used as an aid, in vertical or alveolar ridges. Horizontal preservation had significantly better clinical outcomes. According to the treatment needs, appropriate bone materials were selected for bone ridge preservation and local administration of Vit.D3, and the extraction cavity closure was performed with autologous root slices to observe and track the therapeutic effect. Free gingival grafts or pedicle soft tissue grafts can help bone and spine preservation with good clinical outcomes, but autologous soft tissue grafts can increase wounds at the donor site and increase the patient's postoperative discomfort. Collagen sponges can help bone graft materials. Stay in the extraction cavity, promote the formation and fixation of blood clots, and prevent soft tissue from growing in, but collagen degrades rapidly, and it will decompose faster once the nearby tissue has symptoms of acute inflammation. The advantage of autologous root slices is that it is biocompatible High performance, it can effectively isolate the bone graft material from the contamination of the oral environment, and it will not absorb or be infected due to the acute inflammation of the nearby tissue. Wounds can reduce postoperative discomfort, so the use of autologous tooth root slices without the periodontal ligament exposed to the oral environment is less likely to cause infection or premature absorption, and can effectively protect the stability of blood clots in the extraction cavity. , reduce the saliva contamination of bone graft materials, and at the same time will not increase the cost of materials or the economic burden of the patient, the side with the periodontal ligament can also promote bone formation and help the retention of alveolar bone, which is both novel and good. The method of sealing the extraction socket can improve the predictability and aesthetics of the bone and spine preservation surgery, and help the patient to be replanted in an ideal position in the future. It is also hoped that the effect of Vit.D3 in promoting bone regeneration can accelerate the healing of the extraction socket.

Enrollment

10 patients

Sex

All

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Willing to sign written subject consent to surgery
  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

  1. Patients with potentially impaired healing capacity such as cancer, diabetes, bone infection, tuberculosis, hemoglobin abnormal anemia or congenital immunodeficiency conditions, cellulitis, acute periodontal cysts, severe cusp lesions (cyst size) >2mm2) or subjects with dental and jaw lesions.
  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])

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

10 participants in 4 patient groups

Autologous Tooth Root+Vit.D3+Bone graft
Experimental group
Description:
Placement of bone graft and local administration of Vit.D3, and placement of autologous root slices
Treatment:
Procedure: Autologous Tooth Root
Drug: Vit.D3
Other: bone graft
Autologous Tooth Root+ Bone graft
Experimental group
Description:
Placement of bone graft without local administration of Vit.D3 and placement of autogenous root slices
Treatment:
Procedure: Autologous Tooth Root
Other: bone graft
Bone graft
Experimental group
Description:
Only bone graft materials were placed, no local administration of Vit.D3, and no autologous root slices were placed
Treatment:
Other: bone graft
Natural healing
No Intervention group
Description:
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.

Trial contacts and locations

1

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Central trial contact

Wen H Chi; Hsiang H Hong

Data sourced from clinicaltrials.gov

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