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NCT Number: NCT07373600

Clinical and Radiographic Evaluation of Delayed Dental Implant Placement After Socket Preservation Using Injectable Bone Graft

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.

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Key information

Age range

40 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

  • 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.

Treatment and study plan

Injectable Alloplastic Bone Graft

Device

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 outcomes

  1. 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)

    Implant stability will be assessed at the time of delayed implant placement using resonance frequency analysis (RFA) to obtain implant stability quotient (ISQ) values. The ISQ readings will be used to evaluate the effect of socket preservation with injectable alloplastic bone graft on implant stability in comparison to sites without grafting.

Sponsors and collaborators

Lead sponsor

Suez Canal University

Other

Registry information

Official study title

Clinical and Radiographic Evaluation of Delayed Implant Placement Following Socket Preservation With Injectable Alloplastic Bone Graft. A Randomized Controlled Study.

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jan 28, 2026
Registry last updated
Jan 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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