Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07333534

Hard Tissue Augmentation With or Without Connective Tissue Graft in Immediate Esthetic Implants

Led by University of Baghdad · Updated on 2026-03-13

28

Participants Needed

1

Research Sites

27 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled study is aimed to evaluate the esthetic, clinical, and radiographic outcomes following the placement of immediate single-tooth implant with hard and soft tissue augmentation. Subjects will randomly assigned to one of two groups: * Group A (control group) receiving an immediate single-tooth implant in the esthetic zone with bone augmentation only. * Group B (study group) receiving an immediate single-tooth implant in the esthetic zone with bone augmentation and connective tissue graft (CTG). The main questions it aims to answer is: Is there is a significant difference in the esthetic outcome between bone augmentation alone and bone augmentation combined with connective tissue graft after immediate dental implant in the esthetic zone?

CONDITIONS

Official Title

Hard Tissue Augmentation With or Without Connective Tissue Graft in Immediate Esthetic Implants

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a non-restorable tooth or remaining root without acute infection in the maxillary esthetic zone
  • The failing tooth is an incisor, canine, or first bicuspid in the upper jaw surrounded by natural healthy teeth
  • Have sufficient bone (more than 4 mm) apically and palatally to allow implant placement with primary stability of at least 35 N cm
  • Have enough mesial-distal and interocclusal space for implant placement and restoration
Not Eligible

You will not qualify if you...

  • Have systemic conditions affecting bone healing, such as uncontrolled diabetes
  • Have a tooth with current acute periapical infection
  • Have dehiscence of the facial bone plate after extraction
  • Show signs of uncontrolled periodontal disease
  • Are heavy smokers, pregnant women, or decision-impaired individuals
  • Have a history of head and neck radiation therapy

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

University of Baghdad/ College of Dentistry/ Department of Oral and Maxillofacial surgery/ Implant Unit

Baghdad, Rusafa, Iraq, 10047

Actively Recruiting

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Research Team

K

Khalid Khalid, Bachelor of Dental Surgery

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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