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Trials / Completed

CompletedNCT06027528

Evaluation of Socket Preservation Using Autogenous Dentine Graft With Or Without Autologous Fibrin Glue

Evaluation of Socket Preservation Using Autogenous Dentine Graft With Or Without Autologous Fibrin Glue: A Randomized Controlled Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

* The aim of this interventional study is to investigate the dimensional changes in buccolingual alveolar ridge width in socket preservation using sticky dentin vs dentin graft alone * The main question: is dentin graft mixed with autologous fibrin glue has better dimensional changes than using dentin graft alone ? * outcomes: Change in buccolingual alveolar ridge width as well as apico-coronal alveolar ridge height

Detailed description

* Aim of the study: The aim of this study is to investigate the dimensional changes in buccolingual alveolar ridge width. As well as the apico-coronal alveolar ridge height following tooth extraction when using sticky grafts combined with demineralized dentin grafts for socket preservation. * Research Procedure in brief: This study will be carried out on patients enrolled from the Outpatient Clinic of Oral Medicine and Periodontology department, Faculty of Dentistry, Cairo University. \*operative procedure: Before tooth extraction, probing depths (PD), gingival recession (GR), and bleeding on probing (BOP) will be assessed at six sites (mid-facial, mesio-facial, disto-facial, mid-palatal, mesio-palatal, and disto-palatal) around the tooth to be extracted and on the adjacent teeth to verify their periodontal status. Local anesthesia will be administered by infiltration to achieve the necessary anesthesia to allow extraction of the indicated tooth. Flapless atraumatic extraction will be done. Extracted teeth will be cleaned from periodontal ligaments, cementum, soft tissue attachment, caries or restorations (if present), using a high-speed stone. The pulp chamber will be cleaned with sterile endodontic files. Then, teeth will be grinded to fine particles. The particles prepared will be immersed tooth in alcohol for 10 min for disinfection, then washed twice in saline and dried using sterile gauze. Then the dentine graft particles will be prepared by demineralization of tooth particles in 0.6N hydrochloric acid for 30 min to achieve demineralization then washed twice in saline and dried with sterile gauze Then the patient will be randomly assigned to one of the treatment groups: In group 1 (control group) Demineralized dentine graft will be placed in the socket. In group 2 (test group): Sticky graft preparation will be done as follows: 1. Small amount of patient's venous blood (8-10cc) is drawn via venipuncture, and the blood is placed into non-coated vacutainers to obtain autologous fibrin glue (AFG), which will make sticky graft. 2. The blood in the test tubes is centrifuged at 2700-3000 rpm for 2-3 mins. 3. The upper autologous fibrin glue is obtained with syringe and mixed with particulate of dentine graft and allows for 5-10 minutes for polymerization in order to produce sticky graft. 4. The prepared sticky dentin graft will then be inserted in the socket. * Post operative radiograph: Cone beam CT will be taken post surgically to measure the buccolingual dimension in the same day of the surgery. \*Post-surgical procedure: (six months after socket preservation) Another Cone beam CT will be taken to measure the outcomes by superimposition of the 2 CBCT

Conditions

Interventions

TypeNameDescription
PROCEDUREdentin graft mixed with autologous fibrin glueextracted tooth will be grinded into small particles to form dentin graft that will be mixed with autologous fibrin glue to be grafted in the extracted socket using centrifuge
PROCEDUREdentin graftextracted tooth will be grafted in the socket

Timeline

Start date
2023-09-01
Primary completion
2024-03-21
Completion
2025-08-31
First posted
2023-09-07
Last updated
2026-04-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06027528. Inclusion in this directory is not an endorsement.