Prosthetic and Biological Complications of Implant Supported Prostheses

March 17, 2022 updated by: Eman Gamal Helal, National Research Centre, Egypt

Prosthetic and Biological Complications of Implant Retained Fixed Versus Removable Telescopic Overdentures

complications of implant retained prostheses

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

counting and analyzing the prosthetic and biological complications of the fixed and removable implant retained prostheses in the completely edentulous patients

Study Type

Observational

Enrollment (Anticipated)

30

Contacts and Locations

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

Study Locations

      • Cairo, Egypt
        • Recruiting
        • National Research Centre
        • Contact:
        • Contact:
          • Ahmed Elsisi, associate professor

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

completely edentulous patients

Description

Inclusion Criteria:

  • completely edentulous patients

Exclusion Criteria:

  • medically free adequate bone quality and quantity

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
telescopic overdenture group
patients receiving implant retained telescopic overdentures
fixed group
patients receiving fixed implant prostheses
fixed implant retained prostheses
Other Names:
  • fixed implant prosthses

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
biological complications
Time Frame: one month
biological complications of implant retained prostheses
one month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
prosthetic complications
Time Frame: three months after delivery of the prostheses
prosthetic complications of implant retained prostheses
three months after delivery of the prostheses

Collaborators and Investigators

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

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 (Anticipated)

May 20, 2022

Primary Completion (Anticipated)

December 19, 2022

Study Completion (Anticipated)

December 30, 2022

Study Registration Dates

First Submitted

March 17, 2022

First Submitted That Met QC Criteria

March 17, 2022

First Posted (Actual)

March 28, 2022

Study Record Updates

Last Update Posted (Actual)

March 28, 2022

Last Update Submitted That Met QC Criteria

March 17, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 20199

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

Yes

product manufactured in and exported from the U.S.

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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