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Clinical Trials/NCT06657651
NCT06657651
Enrolling By Invitation
Not Applicable

Autogenous Dentine Derived Barrier Membrane Versus Extended Platelet Rich Fibrin Membrane in Immediate Implant Placement

Mansoura University1 site in 1 country40 target enrollmentJune 30, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tooth Extraction
Sponsor
Mansoura University
Enrollment
40
Locations
1
Primary Endpoint
Implant stability
Status
Enrolling By Invitation
Last Updated
last year

Overview

Brief Summary

forty patients will be selected from the outpatient's clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University for replacement of non-restorable tooth in posterior mandibular area.

Patients' Grouping:

The patients will be randomly divided into two equal uniform groups each consists of 20 patients:

Group A:

20 patients with non-restorable mandibular molar tooth will be treated with an immediately placed dental implant in conjunction with a dentin-derived membrane from the extracted tooth.

Group B:

20 patients with non-restorable mandibular molar tooth will be treated with an immediately placed dental implant in conjunction with extended platelet rich fibrin membrane.

Registry
clinicaltrials.gov
Start Date
June 30, 2024
End Date
June 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age above 18 years
  • Non-restorable mandibular molar tooth that needs dental extraction \& guided bone regeneration for immediate implant placement.
  • Acceptable inter-arch space for the future prosthesis.
  • Patient medically free from systemic diseases that absolutely contraindicate implant surgery.
  • Cooperative patient with high motivation and acceptable oral hygiene.
  • Free from history of bruxism / parafunctional habits.

Exclusion Criteria

  • Local and / or systemic conditions that interfere with the procedure.
  • Pregnancy.
  • Uncooperative patients.
  • Patient had undergone in the past 12 months radiation therapy to the head and neck area.

Outcomes

Primary Outcomes

Implant stability

Time Frame: 1 year

Osstell will be used to record implant stability at the placement time, 3, 6 and 12 months after surgery.

Study Sites (1)

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