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A Comparison Between Protemp and Flowable Light Cure Composite Material for Creating Optimal Gingival Emergence Profile Around Implant

NCT07196293 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-09-29

No results posted yet for this study

Summary

The study focuses on the critical role of the gingival emergence profile in the success of dental implants, emphasizing its importance for both peri-implant health and esthetics. The research aims to evaluate and compare the effectiveness of two common, cost-effective dental materials-light-cure composite and Protemp (a bis-acryl composite resin)-for fabricating customized healing abutments. By assessing the peri-implant tissue response to these materials, the study seeks to determine which is more suitable for creating an optimal, natural-looking soft tissue contour, thereby providing dentists with a practical and reliable alternative to more expensive options like PEEK.

Conditions

  • Customized Healing Abutment
  • Dental Implant
  • Composite Resin
  • Peri-Implant Health

Interventions

PROCEDURE

Customized Healing Abutment - bulk fill composite

instead of standard healing abutments , customization was done using bulk fill composite

PROCEDURE

customized healing abutments - Bis acryl composite materials

customized healing abutments with bis acryl composite material was used instead of standard healing abutments

Sponsors & Collaborators

  • Amrita Institute of Medical Sciences & Research Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-01
Primary Completion
2025-08-30
Completion
2025-08-30

Countries

  • India

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 NCT07196293 on ClinicalTrials.gov