Clinical and Radiographic Evaluation of Delayed Dental Implant Placement After Socket Preservation Using Injectable Bone Graft
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Injectable Alloplastic Bone Graft.
- Who it may be relevant to
- Registry conditions: Alveolar Ridge Preservation, Dental Implant Placement. Basic parameters: 40 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Clinical and Radiographic Evaluation of Delayed Implant Placement Following Socket Preservation With Injectable Alloplastic Bone Graft. A Randomized Controlled Study.
Overview
This clinical study aims to evaluate the clinical and radiographic outcomes of delayed dental implant placement following socket preservation using an injectable alloplastic bone graft material. The study will include patients who require tooth extraction and are candidates for implant placement. After tooth extraction, the socket will be preserved using the bone graft material, and dental implants will be placed after a healing period. Clinical and radiographic assessments will be performed to evaluate bone quality, bone height, and implant stability. The goal of this study is to determine the effectiveness of injectable alloplastic bone grafts in maintaining the alveolar ridge and improving the success of delayed implant placement.
Interventions
- Device Injectable Alloplastic Bone Graft
Following tooth extraction, socket preservation will be performed using an injectable alloplastic bone graft material composed of biocompatible synthetic components. The material will be placed into the extraction socket to maintain ridge dimensions and promote bone regeneration. After a healing period of several months, delayed implant placement will be performed, and clinical and radiographic evaluations will assess ridge preservation and implant success
Primary outcome measures
- Implant stability at the time of delayed implant placement [Time frame: At the time of delayed implant placement (approximately 4 to 6 months after tooth extraction)]
Eligibility criteria
- Patient aged between 40 and 60 years
- General good health.
- Volunteer subjects have to voluntarily sign an informed consent.
- Patient Indicated for single implant placement in lower posterior area.
Inclusion criteria for patients in group I
· Patient with a previously extracted lower posterior tooth and the socket was preserved with injectable bone graft .
Exclusion criteria
- Patient with systemic disease affection bone metabolism .
- Patients with contraindication to surgical treatment.
- Patients with uncontrolled medical conditions.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07373600 · 1004/2025