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

U

University of Baghdad

Status

Not yet enrolling

Conditions

Dental Implant

Treatments

Procedure: Immediate dental implant in the esthetic zone

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

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?

Enrollment

28 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a non-restorable tooth or a remaining root without signs of acute infection in the maxillary esthetic zone.
  • The failing tooth is an incisor, canine or first bicuspid in the maxilla bounded by natural sound teeth.
  • Sufficient bone (>4 mm) apically and palatally to allow for proper implant positioning with sufficient primary stability (≥35 N cm).
  • Sufficient mesial-distal and interocclusal space for placement of the implant and definitive restoration.

Exclusion criteria

  • Patients with systemic conditions affecting bone healing (e.g., uncontrolled diabetes).
  • Teeth with current acute periapical infection.
  • Dehiscence of the labial (facial) bone plate after extraction.
  • Signs of uncontrolled periodontal disease.
  • Heavy smokers and vulnerable groups (pregnant females and decision-impaired individuals).
  • History of head and neck radiation therapy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

28 participants in 2 patient groups

Hard tissue augmentation with connective tissue graft
Experimental group
Description:
Hard tissue augmentation (bone grafting) with additional connective tissue graft (CTG) performed at the same time following immediate dental implant in the esthetic zone
Treatment:
Procedure: Immediate dental implant in the esthetic zone
Hard tissue augmentation
Active Comparator group
Description:
Hard tissue augmentation (bone grafting) following immediate dental implant in the esthetic zone.
Treatment:
Procedure: Immediate dental implant in the esthetic zone

Trial contacts and locations

0

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Central trial contact

Khalid Khalid, Bachelor of Dental Surgery

Data sourced from clinicaltrials.gov

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