Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07315607

In Vivo Evaluation of the Accuracy of Immediate Screw-Retained Provisional Crowns Fabricated Using Digital Planning and Guided Surgery

Led by Universidad Complutense de Madrid · Updated on 2026-01-09

27

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

In Vivo Evaluation of the Accuracy of Immediate Screw-Retained Provisional Crowns Fabricated Using Digital Planning and Guided Surgery

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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 5 Ncm
  • Ability to understand the study procedures and provide written informed consent
  • Willingness to comply with the study protocol and attend required clinical visits
Not Eligible

You will not qualify if you...

  • 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
  • Any other condition that, in the investigator's judgment, could compromise patient safety, protocol adherence, or data validity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Complutense University of Madrid

Madrid, Madrid, Spain, 28040

Actively Recruiting

Loading map...

Research Team

M

Miguel A Gómez Polo ; DDS, PhD, DDS, PhD

CONTACT

S

Solange J Vasquez Ramos, DDS, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here