IMMEDIATE IMPLANT With Different Types of Membranes

NCT06657651 · tracked via the Priya Life Science Egypt tracker

Sponsor

Mansoura University

Phase

Not applicable

Started

2024-06-30

Last updated

2024-10-28

Condition(s) studied

Tooth Extraction

Investigational drug(s) / intervention(s)

immediate implant placement with dentin-derived membraneimmediate implant with extended platelet rich fibrin membrane

immediate implant placement with dentin-derived membrane: immediate implant placement with dentin-derived membrane and allograft in mandibular molar area

immediate implant with extended platelet rich fibrin membrane: immediate implant with extended platelet rich fibrin membrane and allograft in mandibular molar area

Study 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.

Eligibility

Sex

ALL

Min age

18 Years

Max age

60 Years

Healthy volunteers

Accepted

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. * Smokers. * Pregnancy. * Uncooperative patients. * Patient had undergone in the past 12 months radiation therapy to the head and neck area.

Primary outcome measure(s)

Implant stability — 1 year
Osstell will be used to record implant stability at the placement time, 3, 6 and 12 months after surgery.

Trial sites (1)

Facility	City	Region	Status
Heba Elsheikh	Al Mansurah	Egypt

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06657651 on ClinicalTrials.gov ↗ ← All trials in Egypt