Guided Bone Regeneration Using a Mixture of Autogenous and Xenograft Particulate Versus Patient-Specific Sticky Bone for Horizontal Anterior Maxillary Defect

ConditionSticky Bone
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-60
SponsorCairo University

About this trial

This study aims to enhance healing while minimizing invasiveness and restoring tissues to their proper structure and function by using patient specific sticky bone that will enhance the soft tissue reaction and maintain the graft volume stability and bone quality which stabilizes bone grafts, accelerates tissue healing, and reduces bone loss.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients of both genders requiring implants placement in anterior maxilla with horizontal bone defect.

Patients of age older than 20 years old.

Patients with adequate Inter-arch space.

Patients who were willing and fully capable to comply with the study protocol.

Disqualifiers

Heavy smokers (> than 10 cigarettes a day)

Patients with parafunctional habits

Patients with uncontrolled systemic diseases.

Patients with poor oral hygiene

Trial design

Design model

Parallel

Treatments tested in this trial

  • Mixture of Autogenous and Xenograft Particulates

    Procedure/Surgery

    This group will receive guided bone regeneration using a 1:1 mixture of autogenous bone harvested from the mandibular ramus and xenograft bone substitute (e.g., Bio-Oss). The graft material will be covered with a titanium meshes. Standard flap design, fixation, and suturing techniques will be used

  • Patient-Specific Sticky Bone

    Procedure/Surgery

    This group will receive guided bone regeneration using patient-specific sticky bone, created by mixing autogenous bone and xenograft with autologous fibrin glue (PRF). The sticky bone graft will be molded and applied directly to the defect site, covered with a titanium meshes, and stabilized using standard surgical protocol.

Treatment groups

20 Participants
are divided into 2 treatment groups
Group A: Autogenous + Xenograft particulate group.Active comparator 1 intervention
Group B: Patient-specific Sticky Bone group.Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Radiographic and Histomorphometric Assessment for Guided Bone Regeneration using a Mixture of Autogenous and Xenograft Particulate Versus Patient-Specific Sticky Bone for Horizontal Anterior Maxillary Defect (Randomized Clinical Trial)

Time frame
Baseline (preoperative), 6 months postoperative for radiographic evaluation; 6 months postoperative for histomorphometric biopsy assessment at re-entry.
2

Radiographic and Histomorphometric Assessment for Guided Bone Regeneration using a Mixture of Autogenous and Xenograft Particulate Versus Patient-Specific Sticky Bone for Horizontal Anterior Maxillary Defect (Randomized Clinical Trial)

Radiographic outcomes will include CBCT-based measurements of horizontal ridge width and bone volume gain at the grafted sites. Histomorphometric evaluation will be performed using biopsies collected at re-entry to assess new bone formation, residual graft particles, and connective tissue. Comparisons will be made between autogenous/xenograft particulate grafts and patient-specific sticky bone in terms of bone regeneration effectiveness.

Time frame
Baseline (preoperative), 6 months postoperative for radiographic evaluation; 6 months postoperative for histomorphometric biopsy assessment at re-entry.

Secondary outcomes

Other outcomes

Sponsors and contacts

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