Clinical Trial on the Safety and Efficacy of Magnesium Doped Calcium Silicate 3d Alveolar Bone Repair Unit for Periodontal Bone Defects

Alveolar Bone Loss Clinical Trial

Official title:

Clinical Trial on the Safety and Efficacy of Magnesium Doped Calcium Silicate 3d Alveolar Bone Repair Unit for Periodontal Bone Defects

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05743452
• Other study ID #: 2022-0535
• Status: Recruiting
• Phase: Early Phase 1
• Start date: August 18, 2022
• Est. completion date: December 2023

Study information

• Verified date: February 2023
• Source: Second Affiliated Hospital, School of Medicine, Zhejiang University
• Contact: Lili Chen, Prof.
• Phone: 13606507966
• Email: chenlili_1030[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to test in height increment of alveolar bone and safety evaluation index.

The main question it aims to answer are:

• The safety and effectiveness of magnesium calcium silicate three-dimensional alveolar bone repair unit in the repair of periodontal bone defects Participants will be treated through Guided Bone Regeneration operation with calcium magnesium silicate three-dimensional alveolar bone repair unit.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 5
• Est. completion date: December 2023
• Est. primary completion date: December 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Age 18-65 years old, healthy;

• Good oral hygiene, do not smoke;

• There is bone defect at the tooth extraction site, and it is planned to carry out implant repair after tooth extraction;

• There is at least one healthy adjacent tooth in the mesial and distal surface of the tooth extraction site;

• The residual height from the bottom of the extraction socket to the crest of the alveolar ridge is = 3 mm, with at least one bone wall;

• Can understand the purpose of the trial

• Be willing to cooperate with surgical treatment and follow-up, voluntarily participate in the trial

• Sign the informed consent form.

Exclusion Criteria:

• The affected tooth is in the acute inflammatory stage;

• Those who have bad habits such as smoking and drinking;

• Subjects who cause artifacts in oral imaging examination, such as the extraction site and its adjacent teeth are metal Dentures, porcelain teeth;

• Patients are allergic to ceramic implants;

• Those who have participated in other clinical trials in the past 3 months;

• The investigator estimated that the compliance was poor, or there were other factors that were not suitable for the test;

• Patients with a history of diabetes or abnormal blood glucose detection (fasting blood glucose = 7mmol/L);

• Abnormal liver and kidney function (AST, ALT, creatinine = 1.5 times ULN);

• Patients with serious endocrine and metabolic diseases;

• Have a history of tertiary hypertension;

• Have a history of osteoporosis;

• Those who are not suitable for surgery due to the history of malignant tumor or other serious diseases;

• People with a history of autoimmune diseases;

• Pregnant or lactating women;

• Mental disorders without autonomous behavior ability;

• Patients who are using steroids that interfere with calcium metabolism within 3 months before the signing of informed consent

Related Conditions & MeSH terms

• Alveolar Bone Loss

Intervention

Device:
• GBR with CS@Mg
The patient was treated by GBR with magnesium calcium silicate scaffold for alveolar bone defect.

Locations

Country	Name	City	State
China	Department of Oral Medicine, the Second Affiliated Hospital School of Medicine of Zhejiang University	Hangzhou

Sponsors (1)

Lead Sponsor	Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Horizontal bone width	The width of buccal lingual alveolar ridge was measured 1 mm below the crest of alveolar ridge.	24 weeks after operation
Primary	Evaluation of wound healing	The wound healing evaluation scale was modified according to the indicators described by Lobene et al (1986) and will be used to evaluate the wound healing after surgery. The gingival tissue in the material implantation area was evaluated.	2 weeks after operation