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Surface Topography and Color Stability of Conventional, 3D Printed, and Milled Provisional Restorations.

Comparative Assessment of the Color Stability and Surface Roughness of Implant-Supported Provisional Restorations Fabricated by Conventional Technique, Milling and 3D Printing: A Randomized Controlled Clinical Trial.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06946693
Enrollment
36
Registered
2025-04-27
Start date
2025-04-18
Completion date
2027-01-18
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 Implant

Keywords

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, consent 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. Provisional restorations fabricated by conventional technique, milling, and 3D printing will constitute three groups, followed by evaluation of color stability and surface roughness after intraoral use.

Detailed description

Title: Comparative assessment of the color stability and surface roughness of implant-supported provisional restorations fabricated by conventional technique, milling, and 3D printing: A randomized controlled clinical trial Rationale: The study needs to verify the color stability and surface roughness of implant-supported provisional restorations fabricated using conventional technique, milling, and 3D printing. Aim and objectives: To evaluate the color stability and surface roughness of implant-supported provisional prosthesis fabricated using conventional technique, milling, and 3D printing in the mandibular posterior region. Setting: Department of Prosthodontics and Crown & Bridge, PGIDS, Rohtak. Study Design: Randomized controlled clinical trial. Population/Participants: Provisional restoration will be fabricated using conventional technique, milling and 3D printing. Sample Size: Total of 36 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 color stability and surface roughness of implant-supported provisional restorations fabricated using conventional technique, milling, and 3D printing in the mandibular posterior region. Outcome Measures: Measuring the color stability using spectrophotometer and surface roughness using profilometer. Statistical Analysis: Data obtained will 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 the distribution of data.

Interventions

PROCEDURETo evaluate the color stability and surface roughness of implant supported provisional restorations fabricated using conventional technique, milling, and 3D printing in mandibular posterior region.

Subjects with single stage implant placement and early non-functional loading with implant supported provisional restorations fabricated using conventional technique, milling, and 3D printing.

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 reason. \-

Design outcomes

Primary

MeasureTime frameDescription
Surface roughness of implant supported provisional restorations fabricated using conventional technique, milling, and 3D printing.1 year 6 monthsSurface roughness of provisional restorations will be measured using profilometer
Color stability of implant supported provisional restorations fabricated using conventional technique, milling, and 3D printing.1 year 6 monthsColor stability of provisional restorations will be measured using spectrophotometer

Countries

India

Contacts

Primary ContactMANU RATHEE, MASTER OF DENTAL SURGERY
ratheemanu@gmail.com+91 9416141376

Outcome results

None listed

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