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Clinical Trials/NCT05437172
NCT05437172
Completed
Not Applicable

Clinical and Radiographic Evaluation of Autogenous Demineralized Dentin Graft for Ridge Preservation With and Without Injectable Platelet Rich Fibrin (A Randomized Controlled Clinical Trial)

Cairo University1 site in 1 country24 target enrollmentJune 30, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ridge Preservation
Sponsor
Cairo University
Enrollment
24
Locations
1
Primary Endpoint
Radiographic Bucco-lingual ridge width change
Status
Completed
Last Updated
last year

Overview

Brief Summary

Ridge preservation should be considered whenever possible after tooth extraction. Whether implant placement would be performed or for aesthetic consideration at pontic sites when conventional bridge is planned. Ridge preservation aims to maximize the bone formation accompanied with good soft tissue architecture to facilitate implant and prosthetic replacement restoring function, phonetics and aesthetics. the Aim of the study is To evaluate the bucco-lingual ridge width clinically and radiographically, height of buccal and lingual ridges of the socket after application of injectable platelet rich fibrin and autogenous dentin graft.

Registry
clinicaltrials.gov
Start Date
June 30, 2022
End Date
December 15, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Odai Amer Ahmad Hwafdeh

principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years need of at least one single rooted tooth extraction.
  • Non-restorable teeth.
  • Systemically healthy patients.
  • Good oral hygiene, Plaque index less than 15%.
  • Non-smoker or Smoking ≤ 10 cigarettes/day.
  • Cooperative patients able and accept to come for follow up appointments.

Exclusion Criteria

  • Any interim intervention that may have affected any of the outcomes of interest.
  • Pregnant and lactation females.
  • Smoking ˃ 10 cigarettes/day.
  • Patients reporting systemic conditions that may compromise healing or bone metabolism (eg: diabetes).
  • Patients with poor oral hygiene.
  • Any known allergies.

Outcomes

Primary Outcomes

Radiographic Bucco-lingual ridge width change

Time Frame: up to 24 weeks

radiographic measurement

Secondary Outcomes

  • Changes in the height of the socket buccal and lingual ridges.(up to 24 weeks)
  • postoperative pain(immediately after the procedure)
  • Keratinized tissue width(up to 24 weeks)
  • chair time(immediately after the procedure)
  • Patient satisfaction(immediately after the procedure)

Study Sites (1)

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