跳至主要内容
临床试验/NCT06947070
NCT06947070招募中不适用

"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"

Postgraduate Institute of Dental Sciences Rohtak1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
24
试验地点
1
主要终点
Surface topography of provisional restorations.

研究概览

简要总结

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.

详细描述

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).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

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

排除标准

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

研究组 & 干预措施

To evaluate the surface topography and color stability of Group I 3D printing provisional material.

Active Comparator

干预措施: To evaluate the surface topography and color stability of 3D printing provisional material. (Procedure)

To evaluate the surface topography and color stability of Group II 3D printing provisional material.

Active Comparator

干预措施: To evaluate the surface topography and color stability of 3D printing provisional material. (Procedure)

结局指标

主要结局

Surface topography of provisional restorations.

时间窗: 2 years

The surface topography of implant supported provisional restorations fabricated using two different 3D printing materials evaluated using Profilometer.

Color stability of provisional restorations

时间窗: 2 years

The color stability of implant supported provisional restorations fabricated using two different 3D printing materials evaluated using Spectrophotometer.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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