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Effects of Splinted or Non-splinted Single-unit Crowns on Marginal Bone-level Alterations Around Implants

StatusUnknown
PhaseNot applicable
Started
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Record status
This record was last updated April 26, 2022 (before its estimated September 2024 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Changed Registry marked status Unknown (sponsor has not verified the record since Apr 2022); last known: Recruiting
  2. Notable Primary completion date: Sep 2021 to Sep 2024
    • Study completion date: Sep 2025 to Sep 2026
    • Study description expanded, about 166 words
    v3
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date: Sep 2019 to Sep 2021
    • Study completion date: Sep 2022 to Sep 2025
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The microthreaded and platform switched implants could control the stress in the suitable range. The splint would disturb the function. So it is necessary to know whether the splinted single-unit crowns is fit for the adjacent multi-implants. Outcome variables: Splinted single-unit crowns on one side implants and non-splinted single-unit crowns on the other side Materials and method: 80-100 consecutive implants in at least 20 patients would be included for implant- supported restorations in the posterior maxilla or mandibular. All patients would be in general good health. For every patient, the same posterior teeth had lost on both sides for more than 6 months. All patients were treated by the same qualified surgeon. Prosthetics procedure would be performed by an experienced prosthodontist. The two sides were allocated to the test or the control group according to the predefined computer-generated randomization table. Clinical evaluations and radiographic analysis were performed by an oral and maxillofacial radiologist who was not aware of the type of Prosthetics technique that was used.
Trial Details
NCT Number NCT02880891
Lead Sponsor Peking University
Collaborators: Dentsply Sirona Implants and Consumables
Conditions
(from sponsor)
Jaw, Edentulous, Partially
Related terms Jaw, Edentulous, Partially
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov