Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT06645925

Novel Soft Tissue Augmentation Technique Using Free Gingival Graft Simultaneous With Posterior Mandibular Implant

Led by Misr International University · Updated on 2026-01-29

22

Participants Needed

1

Research Sites

112 weeks

Total Duration

On this page

Sponsors

M

Misr International University

Lead Sponsor

I

International Dental Contiuing Education

Collaborating Sponsor

AI-Summary

What this Trial Is About

Presence of keratinized tissue (KT) around dental implants, plays a crucial role in stability and health of peri-implant tissues. Several studies reported that, minimum of 2 mm keratinized tissue width is required to achieve long-term longevity. Insufficient keratinized mucosa leads to biofilm accumulation, soft tissue inflammation, eventually peri-implant mucositis and peri-implantitis. Hence, the aim of the present trial is to evaluate KTW gain, linear and volumetric changes in buccal soft tissue along with hard tissue alterations following implant restoration at sites treated either with delayed implant placement \& simultaneous FGG or the conventional FGG protocol prior to implant placement.

CONDITIONS

Official Title

Novel Soft Tissue Augmentation Technique Using Free Gingival Graft Simultaneous With Posterior Mandibular Implant

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 50 years
  • Missing lower back tooth or teeth with less than 2 mm of keratinized tissue
  • Sufficient alveolar ridge length of 13 to 15 mm to the inferior alveolar nerve
  • Alveolar ridge width of at least 6 mm
  • Able to tolerate surgical periodontal procedures
  • Provided informed consent and agree to one-year follow-up
Not Eligible

You will not qualify if you...

  • Diagnosis of periodontal disease
  • Current or past smoker
  • Pregnant or breastfeeding female
  • Medical conditions that affect surgery such as uncontrolled diabetes or taking intravenous Bisphosphonates
  • Active infection at implant site
  • Parafunctional habits (unusual or harmful oral habits)
  • Shallow vestibule

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

International Dental Continuing Education

Cairo, Egypt, 11347

Actively Recruiting

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Research Team

N

Nourhan G AbdelAziz, Masters degree periodontology

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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