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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05255341
Enrollment
8
Registered
2022-02-24
Start date
2019-07-16
Completion date
2021-09-16
Last updated
2022-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Socket Preservation

Keywords

socket preservation, vascularized interpositional connective tissue graft, alveolar ridge preservation techniques, bovine bone graft, roll pedicle graft

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.

Interventions

PROCEDUREroll pedicle connective tissue graft with bovine bone

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

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
27 Years to 45 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
width of alveolar bonechanges in the Width of alveolar bone were measured at 3& 5 mm at baseline,3 months and 6 monthsTwo 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

MeasureTime frameDescription
gingival thicknesschanges 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.
height of the alveolar crestchanges in height of alveolar crest were measured at baseline, 3 months and 6 monthsCrestal bone height was measured to determine the amount of bone at gain using digora soft ware

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026