Healing of Apicomarginal Defects Using Autograft or Allograft With Collagen Membrane

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorPostgraduate Institute of Dental Sciences Rohtak

About this trial

Apicomarginal defects, which connect apical and marginal bone loss, are difficult to manage surgically due to their limited regenerative potential. Guided tissue regeneration using grafts and collagen membranes may improve outcomes, but the comparative effectiveness of autografts and allografts in these defects is not well established. This randomized clinical trial at PGIDS Rohtak will evaluate 36 patients undergoing endodontic microsurgery, assigning them to either autograft or allograft combined with a bioresorbable collagen membrane. Clinical and CBCT-based radiographic healing will be monitored over 12 months. The study aims to determine whether allografts can achieve bone regeneration comparable to autografts, offering a less invasive option for treating apicomarginal defects.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Guided tissue regeneration

    Procedure/Surgery

    All participants will undergo standardized endodontic microsurgery to manage apicomarginal defects. After flap reflection, defect debridement, root-end preparation, and retrograde filling, patients will be randomly assigned to one of two groups. Autograft + Collagen Membrane Group and Allograft + Collagen Membrane Group

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Apicomarginal defects treated with allograft and membrane combinationExperimental treatment 1 intervention
Group B: Apicomarginal defects treated with autograft and membrane combinationActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

2D and 3D Radiographic Healing

Volumetric bone fill in the apicomarginal defect, assessed using standardized CBCT imaging at baseline and 12 months. Bone regeneration will be quantified through CBCT-based volumetric analysis to compare healing between the autograft and allograft groups.

Time frame
12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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Postgraduate Institute of Dental Sciences Rohtak

Lead sponsor

Post Graduate Institute of Dental Sciences

Collaborator

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