Surgical Guided Fabricated From Two Different Printing Materials

October 3, 2024 updated by: Suez Canal University

Comparative Assessment for the Positional Accuracy of Dental Implants Inserted by Computerized Surgical Guides Fabricated From Different Printing Materials

implant will be inserted in patients with kennedy class 3 or 4 partially edentulous mandible .the implants will be inserted using teeth supported surgical guide fabricated from two different materials

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Patients with skeletal Angle´s class I maxilla-mandibular relationship,
  2. adequate inter-arch distance, have Kennedy class 3 or 4 partially edentulous mandible of more than 2 teeth missed and will be applied for the treatment of tooth loss and requiring fixed prosthodontic rehabilitation
  3. normal Physical and psychological status to tolerate conventional implant procedures,
  4. Their residual ridge had sufficient bone volume for implant installation and was covered by firm mucoperiosteum.

Exclusion Criteria:

  1. Smokers.
  2. Patients undergoing chemotherapy or radiotherapy and immunocompromised patients.
  3. Patients with, systemic disease that might complicate post-operative healing or contribute to bone resorption, e.g uncontrolled diabetes, psychological disorders, or alcohol, tobacco, or drug abuse
  4. parafunctional habits, poor oral hygiene, limited mouth opening, severe alveolar bone deficiencies,

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: group A implant inserted by stainless steel surgical guide
Device: stainless steel printed surgical guide
the patient will wear the stainless steel surgical guide for the insertion of one implant
Active Comparator: group B implant inserted by resin surgical guide
Device: resin printed surgical guide
the patient will wear the resin surgical guide for insertion of adjacent another implant implant

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
linear deviation of inserted implant
Time Frame: 1 month
coronal and apical deviation of inserted implant from virtually planned one in millimeter.
1 month
angular deviation of inserted implant
Time Frame: 1 month
angular deviation of inserted implant from virtually planned one in angles.
1 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Suez Canal University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

October 1, 2024

Primary Completion (Estimated)

November 1, 2024

Study Completion (Estimated)

November 1, 2024

Study Registration Dates

First Submitted

October 1, 2024

First Submitted That Met QC Criteria

October 3, 2024

First Posted (Actual)

October 8, 2024

Study Record Updates

Last Update Posted (Actual)

October 8, 2024

Last Update Submitted That Met QC Criteria

October 3, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 802/2024

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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