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临床试验/CTRI/2025/09/095367
CTRI/2025/09/095367尚未招募3 期

Comparative Evaluation of Occlusion and Disocclusion Times in Fixed Partial Dentures with Milled and 3D Printed PMMA Prostheses: A Randomized Clinical Trial

prasanna kumar p s1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年10月8日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
typically focuses on the occlusion and disocclusion times, which assess the functional efficiency and timing of bite closure and release with the prostheses.

研究概览

简要总结

This randomized clinical trial aims to compare the occlusion and disocclusion times of fixed partial dentures fabricated using milled versus 3D printed polymethyl methacrylate (PMMA) prostheses. The study will assess the functional performance and efficiency of the two fabrication methods in restoring occlusal function in patients requiring fixed partial dentures. Secondary outcomes include prosthesis retention, stability, patient satisfaction, mechanical complications, and biological responses. Participants will be adult patients with good oral health, suitable for fixed partial denture rehabilitation, and will be randomly assigned to receive either milled or 3D printed PMMA prostheses. Outcomes will be measured at baseline, immediately post-placement, and during follow-ups at 1 week, 3 weeks, 3 months, 6 months to evaluate both short-term adaptation and long-term clinical performance. This study is designed to provide evidence on the comparative effectiveness of these emerging fabrication technologies to guide clinical decision-making in prosthodontics.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • who is requiring fixed partial dentures, who have good oral hygiene and healthy periodontal status.
  • Participants should have adequate bone support and stable occlusion, with no active oral infections or untreated dental diseases.
  • They must be able to provide informed consent and comply with the study protocol and follow-up visits.

排除标准

  • who have implant-retained or implant-supported overdentures and removable partial dentures, as well as those with insufficient clinical data.
  • Additionally, individuals with systemic diseases or conditions affecting oral health, active oral infections, untreated periodontal disease, allergies or sensitivities to the prosthetic materials, and those unable to comply with the study protocol or follow-up requirements are excluded.

结局指标

主要结局

typically focuses on the occlusion and disocclusion times, which assess the functional efficiency and timing of bite closure and release with the prostheses.

时间窗: 0 days,1week,3 week,3 months,6 months

次要结局

  • prosthesis retention and stability, patient satisfaction regarding aesthetics and comfort, mechanical complications(0 days,1week,3 week,3 months,6 months)

研究者

发起方
prasanna kumar p s
申办方类型
Other [self sponsored]
责任方
Principal Investigator
主要研究者

Prasanna kumar PS

Saveetha dental college

研究点 (1)

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