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Comparison Between Two Different Healing Abutments in Single Posterior Implants

NCT06682559 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2025-08-05

No results posted yet for this study

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.

Conditions

  • Dental Implants
  • Dental Implants, Single-tooth

Interventions

OTHER

Prefabricated healing abutment with scan peg

12 participants will receive single posterior implants by fully guided implant protocol followed by placement of prefabricated healing abutment with scan peg having convex emergence profile

OTHER

Customized healing abutment

12 participants will receive single posterior implants by fully guided implant protocol followed by placement of custom healing abutment having concave emergence profile

Sponsors & Collaborators

  • Alexandria University

    lead OTHER

Principal Investigators

  • Mervat E Abdellah · Alexandria University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-01
Primary Completion
2025-05-01
Completion
2025-10-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06682559 on ClinicalTrials.gov