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Comparison Between Two Different Healing Abutments in Single Posterior Implants

Not Applicable
Recruiting
Conditions
Dental Implants
Dental Implants, Single-tooth
Registration Number
NCT06682559
Lead Sponsor
Alexandria University
Brief Summary

The aim of this randomized clinical trial is to evaluate the volumetric analysis of peri-implant soft tissues after 3 months of the use of a prefabricated healing abutment with scan peg in comparison to customized healing abutment.

Detailed Description

Volumetric analysis of peri-implant soft tissues after 3 months of the use of a prefabricated healing abutment with scan peg with convex emergence profile in comparison to customized healing abutment with concave emergence profile.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Adult patients who are classified as ASA I or II physical status and require mandibular single implants (single missing mandibular posterior teeth) with:

    1. Proper bone height and width.
    2. Adequate zone of keratinized tissue (at least 2 mm)
Exclusion Criteria
  • Any systematic disease as uncontrolled diabetes mellitus or metabolic bone diseases
  • Pregnancy and Lactation
  • A history of head and neck radiation treatment.
  • Chronic periodontal diseases.
  • Poor oral hygiene (Silness-Löe plaque index score 2 and 3)
  • Parafunctional habits.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Measurement of peri-implant soft tissues volume3 months

Each participant will undergo volumetric analysis of peri-implant soft tissues after 3 months healing either after using prefabricated healing abutment with scan peg in comparison to customized healing abutment using a 3D meteorology software (GOM inspect). It will be measured in millimeter cube

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Faculty of Dentistry, Alexandria University, Egypt

🇪🇬

Alexandria, Egypt

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