An interventional study of Injectable Alloplastic Bone Graft in Alveolar Ridge Preservation and Dental Implant Placement, sponsored by Suez Canal University. Not yet recruiting. Open to participants aged 40 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-28.
Sponsored by Suez Canal University · Not applicable, Interventional, and Treatment
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.
Suez Canal University is the lead sponsor of 157 studies on the registry; 37 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Inclusion criteria for patients in group I
Exclusion criteria:
Extraction sites left to heal naturally without any bone grafting material before delayed implant placement. Dental implants will be placed after the natural healing period, and clinical and radiographic evaluations will be performed to assess ridge dimensions and implant outcomes
Extraction sockets will be preserved using an injectable alloplastic bone graft material immediately after tooth extraction. After a healing period, delayed implant placement will be performed. Clinical and radiographic measurements will be used to evaluate ridge preservation and implant success.
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
Implant stability at the time of delayed implant placement
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.
Time frame: At the time of delayed implant placement (approximately 4 to 6 months after tooth extraction)
No study locations are listed for this record.
Documents are hosted by the registry — open the source record to download them.
This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Suez Canal University