Skip to main content
OpenTrials
Completed

NCT Number: NCT04321109

Alveolar Ridge Preservation Using Collagen Material and Allograft

Seven Patients who need implants to replace non-restorable teeth in the esthetic zone.

Intervention Group (1): Seven extraction sockets that received the collagen matrix (Collagen cone) for alveolar ridge preservation.

Comparison Group (2): Seven extraction sockets that were treated with mineralized cortico-cancellous bone allograft for alveolar ridge preservation.

Outcome

1. Alveolar ridge preservation both in height and in width to improve implant success rate

* The height of alveolar ridge was assessed clinically using a periodontal probe. * The width of the alveolar ridge was measured after three months after extraction using a caliper clamp. * Changes in the width and height of alveolar bone were evaluated in merged axial and sagittal views using the I-CAT superimposition system (CBCT).

2- Evaluation of newly formed bone quality was performed by histological examination and histomorphometric analysis.

3- Immuno-histochemical staining was done using polyclonal antibody to detect (BMP-2) marker of bone formation

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

The aim of the present study was to compare three months post-extraction augmented ridge using collagen matrix versus mineralized cortico-cancellous bone allograft. This comparison was done clinically, histologically, immunohisto-chemically and radiologically.

  • Clinical parameters included; vertical bone height and bone width that were recorded at baseline and at three months after extraction. Moreover, histomorphometric parameters included; area fraction of osteoid and mature bone three months after extraction by histomorphometric analysis. Immunohistochemical analysis using polyclonal antibody to detect BMP-2 marker of bone formation. Radiographic parameters included superimposition of baseline CBCT, three months after extraction and another one six months after loading with subsequent measurement of bone height, bone width and bone density.

A core biopsy was taken three months after tooth extraction which has undergone histomorphometric and immunohistochemical analysis; implant placement was also done at the same time.

In the present study, it was found that the mean bone height decreased with a higher percent in collagen matrix group than mineralized cortico-cancellous bone allograft group with a non significant difference between both groups.

In addition, this study showed that the mean bone width decreased more in collagen matrix group than mineralized cortico-cancellous bone allograft group with a non significant difference between them.

Moreover, in the present study, Histomorphometric analysis revealed new bone trabeculae formation with osteoblastic rimming, the surrounding fibrous tissue is cellular and remnants of the graft materials was detected , with no marked difference in the amount of newly formed bone between two groups .

Regarding immunohistochemical analysis in both groups, the osteoblasts in the fibrous tissue and osteocytes in newly formed bone are showing nuclear staining, with increasing area of immunopositive cells in mineralized cortico-cancellous bone allograft group.

Radiographically, CBCT superimposition revealed that a greater percent decrease in bone height was denoted in collagen matrix than mineralized cortico-cancellous bone allograft group with a significant difference between both groups after 3 and 6 months.

Accordingly bone width showed a higher decrease in mineralized cortico-cancellous bone allograft group than Collagen matrix group with a non significant difference between both groups after 3 and 6 months.

Finally, bone density showed a greater decrease in Collagen matrix group than mineralized cortico-cancellous bone allograft group with a non significant difference after 3 months but significant difference was found after 6 months between both groups.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients were medically free .
  • Two teeth indicated for extraction due to either severe decay, tooth fracture or failed endodontic treatment.

Exclusion criteria

  • Patients with poor oral hygiene or not willing to perform oral hygiene measures.
  • Pregnant and breast-feeding females.
  • Smokers , Teeth with periodontal or periapical infections.
  • Patients with malocclusion.
  • All patients who had known contraindication to dental implant surgery (e.g: bleeding tendency, radiotherapy, taking bisphosphonate)

Treatment and study plan

Allograft

Other

Corticocancellous mineralized allograft

Collagen cone

Other

Collagen matrix

Primary outcomes

  1. clinical score

    Time frame: change from baseline at 12 weeks

    Dimensional changes in alveolar ridge after alveolar ridge preservation both clinically and radiographically

Secondary outcomes

  1. BMP-2

    Time frame: detected at 12 weeks

    Bone morphogenic protein -2 immunopositive cells in immunostained sections

Sponsors and collaborators

Lead sponsor

Yasmine Fouad

Other

Registry information

Official study title

Alveolar Ridge Preservation Using Collagen Material and Allograft: A Randomized Controlled Trial

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Mar 25, 2020
Registry last updated
Sep 23, 2022

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.

Published trials that share one or more normalized conditions with this study.