IMMEDIATE IMPLANT With Different Types of Membranes

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.

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Key information

Conditions

Tooth Extraction

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Heba Elsheikh

Al Mansurah, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

immediate implant placement with dentin-derived membrane

Procedure

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

immediate implant with extended platelet rich fibrin membrane

Procedure

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

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.

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

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

Important dates

Study start: 2024
Primary completion: 2025
Study completion: 2025
First posted: Oct 24, 2024
Registry last updated: Oct 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

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