Prevention of bone resorption after tooth extraction by using bone substitutes

Not yet recruiting

• Conditions: Subjects chosen will be the ones who have been advised extraction of teeth because of dental caries or trauma.They will otherwise not have any positive medical history.; Abnormal results of function studies of other organs and systems,

• Registration Number: CTRI/2020/01/022753
• Lead Sponsor: Rishiraj College of Dental Science and Research Centre

Brief Summary

This is a randomised, single blinded, parallel group, control, clinical trial comparing the effectiveness of bone grafting materials for socket preservation.Subjects who are advised extraction due to trauma or dental caries will be broadly grouped into three . After doing atraumatic extraction under local anaesthesia, in  group 1: Beta -TCP in combination with HC and ,in group 2: HC alone will be inserted with light pressure and stabilised by suturing.The patients will then be directed to the CBCT centre for bone analysis and this will form the baseline readings.It will record the alveolar bone width and height both buccally and lingually.The patient will then be recalled after 8weeks and another CBCT scan will be done for the same site.There will be a control group , in which no bone grafting will be added. It has been hypothesized that there will be effective bone formation observed after 8weeks in sockets with bone grafting materials and there will be minimal difference between the two materials inserted. This ridge preservation will help in giving prosthesis like implants, thus restoring the architecture ,occlusion, function and esthetics.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-01-15
• Last Update Posted: 2020-01-24

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• 1. Patients indicated for extraction because of caries and trauma.
• 2. Mandibular single rooted tooth or teeth.
• 4. No alcohol or drug abuse.

Exclusion Criteria

• 1. Alveolar bone fracture due to extraction or any other reasons.
• 2. Pregnancy.
• 3. known history with diabetes mellitus, osteoporosis and blood dyscrasis.
• 4. Known allergy to foreign material or Local anaesthetics.
• 6. Traumatic extractions.
• 7. Patients on Bisphosphonates drugs.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Effective alveolar ridge preservation with bone grafting materials used in combination and alone.	8 weeks

Secondary Outcome Measures

Name	Time	Method
Adequate bone will be preserved for prosthesis or replacement of the missing tooth in future in both the groups.	8 weeks

Trial Locations

Locations (2)

Diya Dental Imaging Centre; 🇮🇳 Bhopal, MADHYA PRADESH, India

Rishiraj College of Dental Science and Research centre; 🇮🇳 Bhopal, MADHYA PRADESH, India

Diya Dental Imaging Centre

🇮🇳Bhopal, MADHYA PRADESH, India

Dr P Jaju

Principal investigator

9752093011

diyadentalimaging@gmail.com