Evaluation of Bone Regenerated With Guided Bone Regeneration (GBR) Using Polymethylmethacrylate (PMMA) Membrane

NCT06186232 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2024-08-21

No results posted yet for this study

Summary

To evaluate the quantity and quality of bone generated, radiographically and histomorphometrically, after guided bone regeneration (GBR) using a membrane of 3D printed custom made (PMMA) and subsequent stability of delayed implant placement.

Conditions

  • Horizontal Ridge Deficiency

Interventions

PROCEDURE

guided bone regeneration (GBR).

guided bone regeneration (GBR) using polymethylmethacrylate (PMMA) polymer as membrane.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Hesham El Hawary · Professor of Oral and Maxillofacial surgery, Cairo university

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-01
Primary Completion
2025-06-01
Completion
2025-12-01

More Related Trials

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 NCT06186232 on ClinicalTrials.gov