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Surface Topography and Color Stability of Implant Supported 3D Printed Provisional Restorations

Comparative Evaluation of Surface Topography and Color Stability of Implant Supported Provisional Restorations Fabricated Using Two Different 3D Printing Materials in Mandibular Posterior Region: A Randomized Clinical Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06947070
Enrollment
24
Registered
2025-04-27
Start date
2023-07-01
Completion date
2025-04-30
Last updated
2025-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

DENTAL IMPLANTATION

Keywords

3D printed provisional restorations

Brief summary

Patient attending the Outdoor Patient Department of the Department of Prosthodontics at Post Graduate Institute of Dental Sciences, Rohtak will be screened. The screening will include history taking and clinical examination of the partially edentulous patients. Patients will be selected according to the inclusion and exclusion criteria. Single stage endosseous implants will be placed. Two different Biocompatible 3D printed Polymethyl methacrylate resin will constitute two groups, Group A and Group B. 3D printed provisional poly methyl methacrylate resin crowns will be fabricated with Group- A and Group-B material followed by evaluation of surface topography and color stability after intraoral use.

Detailed description

Title: Comparative Evaluation of Surface Topography and Color Stability of Implant Supported Provisional Restorations Fabricated using Two Different 3D Printing Materials in Mandibular Posterior Region: A Randomized Clinical Trial. Rationale: The study needs to verify the surface topography and color stability of implant supported provisional restorations fabricated using two different 3D printing materials in mandibular posterior region. Aim and objectives: To evaluate the surface topography and color stability of implant supported provisional restorations fabricated using two different 3D printing materials in mandibular posterior region. Setting: Department of Prosthodontics and Crown & Bridge, PGIDS Rohtak. Study Design: Randomised clinical trial. Population/Participants: Provisional restoration will be fabricated using two different 3D printing materials. Sample Size: Total of 24 samples will be prepared (n=12 samples per test group). Methodology: This is an in-vivo study and will be carried out in the Department of Prosthodontics and Crown & Bridge, Post Graduate Institute of Dental Sciences, Rohtak with the purpose to evaluate the surface topography and color stability of implant supported provisional restorations fabricated using two different 3D printing materials in mandibular posterior region. Outcome Measures: Measuring the surface topography using profilometer and color stability using spectrophotometer. Statistical Analysis: Data obtained would be compiled on MS Office Excel Sheet (v 2010) and will be subjected to statistical analysis using statistical package for social sciences (SPSS v 21.0, IBM). Intergroup and intragroup comparisons will be done according to distribution of data.

Interventions

PROCEDURETo evaluate the surface topography and color stability of 3D printing provisional material.

Subjects with single stage implant placement followed by early non-functional loading with implant supported provisional restorations fabricated using 3D printing provisional material.

Sponsors

Postgraduate Institute of Dental Sciences Rohtak
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. Subjects consented to participate in the study. 2. Subjects with maintainable oral hygiene. 3. Subjects with adequate edentulous space at the prospective implant site. 4. Subjects with availability of adequate quantity and quality of bone.

Exclusion criteria

1. Subject with presence of infection around proposed site of implant placement. 2. Subjects with any condition that would interfere with the soft tissue and bone healing. 3. Subjects in which surgical procedure is contraindicated for any reasons.

Design outcomes

Primary

MeasureTime frameDescription
Surface topography of provisional restorations.2 yearsThe surface topography of implant supported provisional restorations fabricated using two different 3D printing materials evaluated using Profilometer.
Color stability of provisional restorations2 yearsThe color stability of implant supported provisional restorations fabricated using two different 3D printing materials evaluated using Spectrophotometer.

Countries

India

Contacts

Primary ContactManu Rathee, MDS
ratheemanu@gmail.com09416141376

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026