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Clinical Trials/NCT05255341
NCT05255341
Completed
Not Applicable

Clinical and Radiographic Evaluation of the Effect of Socket Preservation Using the Roll Pedicle Connective Tissue Graft With Bovine Bone: A Case Series Trial.

Cairo University1 site in 1 country8 target enrollmentJuly 16, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Socket Preservation
Sponsor
Cairo University
Enrollment
8
Locations
1
Primary Endpoint
width of alveolar bone
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

After tooth extraction, the residual alveolar ridge generally provides limited bone volume because of ongoing, progressive bone resorption. Healing events within post-extraction sockets reduce the dimensions of the socket over time. Therefore, socket preservation became an indispensable procedure as well as fundamental to prevent bone loss following tooth extraction. Preservation, by the name, is the maintenance of the socket, which is essentially the height and width of the gap that is left after the tooth is removed. It is done by placing a graft material or scaffold immediately into the socket of an extracted tooth to presto preserve bone height, width and density

Detailed Description

Investigator evaluate the clinical and radio graphic effect of roll pedicle connective tissue graft as a barrier membrane together with bovine bone in alveolar ridge preservation in extraction sockets.

Registry
clinicaltrials.gov
Start Date
July 16, 2019
End Date
September 16, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Noha Magdy Salem Amen Eladly

principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • • patients with healthy systemic condition.
  • Adult patients ˃ 18 years old.
  • hopeless teeth that need tooth or root extraction in the maxillary esthetic zone.
  • Alveolar socket Grade I and II.
  • Normal platelet counts according to complete blood count (CBC) test done in the screening stage.

Exclusion Criteria

  • Acute infection at the extraction site
  • Smokers ˃ 10 cigarettes / day.
  • Medications that may interfere with wound healing
  • History of treatment with bisphosphonates.
  • History of allergic reaction

Outcomes

Primary Outcomes

width of alveolar bone

Time Frame: changes in the Width of alveolar bone were measured at 3& 5 mm at baseline,3 months and 6 months

Two holes will be made in the acrylic stent (3mm and 5 mm below the alveolar crest) on the buccal and palatal extensions within the midline of the tooth to be extracted. The buccopalatal width of the alveolar ridge will be measured at the two assigned points using bone caliper at baseline and 6 months post extraction

Secondary Outcomes

  • height of the alveolar crest(changes in height of alveolar crest were measured at baseline, 3 months and 6 months)
  • gingival thickness(changes in the gingival thickness were measured at 3 & 5mm at (baseline,3 months and 6 months))

Study Sites (1)

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