About this trial

This randomized controlled clinical trial aims to compare peri-implant hard and soft tissue dimensional changes following immediate implant placement with the socket shield technique and immediate restoration versus early type II implant placement with contour graft in the esthetic zone. The primary outcome is the Pink Esthetic Score (PES), while secondary outcomes include mid-facial mucosal recession, radiographic vertical and horizontal buccal bone remodeling, and patient satisfaction after 12 months.

Eligibility criteria

Qualifiers

Adults aged 18 years or older

Patients presenting with a single non-restorable tooth in the esthetic zone indicated for extraction and implant replacement

Presence of a thin buccal bone plate (<1 mm)

Adequate bone volume to allow implant placement in a prosthetically ideal position

Disqualifiers

History of systemic diseases that may affect bone healing

Use of medications that may influence bone metabolism (e.g., bisphosphonates)

Smoking within the past 5 years

Presence of acute infection at the surgical site or adjacent teeth

Trial design

Treatments tested in this trial

  • Socket Shield
  • Early Implant Placement

Treatment groups

42 Participants
are divided into 2 treatment groups

Locations

1
Gulf Medical University4184, Ajman United Arab Emirates

Sponsors and collaborators

Gulf Medical University

Lead sponsor