Evaluation of "Tent-Pole" Grafting Technique for Reconstruction of Mandibular Ridge Vertical Defects

NCT04192851 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2020-07-28

No results posted yet for this study

Summary

The aim of this study is to evaluate clinically and radio-graphically the efficiency of "Tent- Pole "grafting technique for reconstruction of anterior or posterior mandibular ridge defects using synthetic bone graft and Platelet Rich Fibrin (PRF) membrane.

Conditions

  • Jaw Deformity

Interventions

PROCEDURE

Tent Pole Technique

* All patients were operated under local or general anaesthesia according to the case and patient tolerability. * The oral cavity was prepared by 0.12% chlorhexidine mouthrinses solution\* for thirty seconds. * Full thickness incision down to the bone with blade no.15. * A periosteal elevator was used to perform mucoperiosteal flap. * Gentle elevation of the flap * Fixation of the screws over the alveolar ridge with about 5 mm of the screw threads will be exposed * Bone graft was mixed with the patient blood and placed to cover the screws completely. * PRF membrane was be placed over the grafted sites. * Repositioning of the flap and suturing with 3/0 black silk suture material

Sponsors & Collaborators

  • Alexandria University

    collaborator OTHER
  • Nourhan M.Aly

    lead OTHER

Principal Investigators

  • Asmaa M Abd ElFattah, BDS · Faculty of Dentistry, Alexandria University, Egypt

  • Abd El Aziz F Khalil, PhD · Faculty of Dentistry, Alexandria University, Egypt

  • Lydia N.F Melek, PhD · Faculty of Dentistry, Alexandria University, Egypt

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-20
Primary Completion
2019-11-15
Completion
2019-11-30

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04192851 on ClinicalTrials.gov