In Vivo Evaluation of the Accuracy of Immediate Screw-Retained Provisional Crowns Fabricated Usin… (NCT07315607) | Clinical Trial Compass
RecruitingNot Applicable
In Vivo Evaluation of the Accuracy of Immediate Screw-Retained Provisional Crowns Fabricated Using Digital Planning and Guided Surgery
Spain27 participantsStarted 2026-01
Plain-language summary
This clinical trial aims to evaluate the in vivo accuracy of a fully digital workflow for the immediate placement of a previously fabricated screw-retained provisional crown using digital planning and guided implant surgery. The study will be conducted in partially edentulous adult patients requiring the replacement of a single tooth with an immediately loaded dental implant.
The main objective of the study is to assess the accuracy (trueness and precision) of the planned digital implant position and provisional restoration by comparing the virtually planned position with the actual clinical outcome after guided surgery. Emphasis will be placed on linear, angular, and rotational deviations at both the implant and provisional restoration levels.
Participants will undergo a fully guided implant placement procedure with rotational control, followed by the immediate placement of a prefabricated screw-retained provisional crown designed during the digital planning phase. Postoperative intraoral scans will be obtained to register the final implant and restoration positions.
The planned and achieved positions will be compared using three-dimensional analysis software to quantify deviations and determine whether the accuracy achieved remains within clinically acceptable limits.
Who can participate
Age range18 Years
SexALL
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Inclusion criteria
✓. Adults aged 18 years or older.
✓. Partially edentulous patients requiring replacement of a single tooth with an immediately loaded dental implant.
✓. Patients classified as ASA I or ASA II according to the American Society of Anesthesiologists physical status classification.
✓. Patients with clinical conditions allowing immediate implant placement with a minimum primary stability of ≥25 Ncm.
✓. Ability to understand the study procedures and provide written informed consent.
✓. Willingness to comply with the study protocol and attend required clinical visits.
Exclusion criteria
✕. Patients classified as ASA III or ASA IV, or with uncontrolled systemic conditions that may interfere with study participation.
✕. Presence of psychiatric or cognitive disorders that may compromise informed consent or protocol compliance.
✕. Inability to comply with the visit schedule or required evaluations.
What they're measuring
1
Accuracy of Implant and Provisional Crown Placement