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

Socket Preservation Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05255341
• Other study ID #: roll pedicle graft
• Status: Completed
• Phase: N/A
• Start date: July 16, 2019
• Est. completion date: September 16, 2021

Study information

• Verified date: February 2022
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 8
• Est. completion date: September 16, 2021
• Est. primary completion date: March 1, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 27 Years to 45 Years

Eligibility

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

Related Conditions & MeSH terms

• Socket Preservation

Intervention

Procedure:
• roll pedicle connective tissue graft with bovine bone
rotated pedicle connective tissue graft together with bovine bone applied for socket preservation after tooth extraction

Locations

Country	Name	City	State
Egypt	Faculty of Dentistry -Cairo University	Giza

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	width of alveolar bone	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	changes in the Width of alveolar bone were measured at 3& 5 mm at baseline,3 months and 6 months
Secondary	gingival thickness	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.	changes in the gingival thickness were measured at 3 & 5mm at (baseline,3 months and 6 months)
Secondary	height of the alveolar crest	Crestal bone height was measured to determine the amount of bone at gain using digora soft ware	changes in height of alveolar crest were measured at baseline, 3 months and 6 months