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

Not Applicable

Completed

• Conditions: Socket Preservation

• Registration Number: NCT05255341
• Lead Sponsor: Cairo University

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.

Study Timeline

• Study Start: 2019-07-16
• Primary Completion: 2021-03-01
• Study Completion: 2021-09-16
• Status Verified: 2022-02
• Study First Submitted: 2022-02-08
• Study First Submitted QC: 2022-02-23
• Study First Posted: 2022-02-24
• Last Update Submitted: 2022-02-24
• Last Update Posted: 2022-03-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 8

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
width of alveolar bone	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 Outcome Measures

Name	Time	Method
height of the alveolar crest	changes in height of alveolar crest were measured at baseline, 3 months and 6 months	Crestal bone height was measured to determine the amount of bone at gain using digora soft ware
gingival thickness	changes in the gingival thickness were measured at 3 & 5mm 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 gingival thickness will be evaluated by William's graduated periodontal probe inserted horizontally perpendicular to the alveolar bone at the two assigned holes labially/buccally at baseline and 6 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 gingival thickness will be evaluated by William's graduated periodontal probe inserted horizontally perpendicular to the alveolar bone at the two assigned holes labially/buccally at baseline and 6 months post extraction.; months post extraction.

Trial Locations

Locations (1)

Faculty of Dentistry -Cairo University; 🇪🇬 Giza, Egypt