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Effect of Metal Artifacts Reduction Orotocols and Electric Potential Difference on Metal Artifacts in Cone Beam Computed Tomography (DTA)

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ClinicalTrials.gov Identifier: NCT03726970
Recruitment Status : Recruiting
First Posted : November 1, 2018
Last Update Posted : April 24, 2019
Sponsor:
Information provided by (Responsible Party):
Marina Salib, Cairo University

Brief Summary:
The effect of metal artifacts reduction protocols and tube potential difference on the metallic artifacts in cone beam computed tomography

Condition or disease Intervention/treatment Phase
Metal Artifacts Radiation: CBCT radiation Not Applicable

Detailed Description:
Our study is a quantitative as well as a qualitative assessment of the metal artifacts in the CBCT images in a bio models with multiple adjacent dental implants and single isolated implants , while using different MAR protocols inherited in the CBCT soft ware , as well as change in the tube potential difference of the CBCT unit

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 2 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Diagnostic
Official Title: Effect of Metal Artifacts Reduction Protocols and Tube Potential Difference on Metal Artifacts in Cone Beam Computed
Actual Study Start Date : September 10, 2018
Actual Primary Completion Date : October 30, 2018
Estimated Study Completion Date : December 10, 2019

Arm Intervention/treatment
Experimental: Tube Potential difference
Different kVp values of the CBCT machine 70, 80 ,90 kVp
Radiation: CBCT radiation
CBCT scanning

Experimental: MAR tool
MAR option in the software off and on
Radiation: CBCT radiation
CBCT scanning




Primary Outcome Measures :
  1. Dental implant linear measurement [ Time Frame: 1 month ]
    The implant length and width in millimeters will be assessed in the presence of the artifacts with and without the activation of the MAR tool of the CBCT soft ware, also change in the potential difference will be done with and without the activation of MAR tool


Secondary Outcome Measures :
  1. Bone- implant interphase [ Time Frame: 1 month ]
    Qualitative assessment if bone - implant interphase, will be either zero or 1 zero indicate that bone implant interphase cannot be assessed , one indicate that the bone implant interphase can be assessed



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • bio models of a lower jaw Titanium implants Porcelain fused to metal crowns

Exclusion Criteria:

-


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03726970


Contacts
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Contact: Marina BB Salib 01226199248 marinasalib@yahoo.com
Contact: Kirollos Yl Youssef 01227199987 Kirollosyoussef@gmail.com

Locations
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Egypt
Marina Salib Recruiting
Cairo, Giza, Egypt, 12511
Contact: Marina BB Salib, BDS    01226199248    marinasalib@yahoo.com   
Contact: Kirollos YL Youssef, BDS    01227199987    Kirollosyoussef@gmail.com   
Sponsors and Collaborators
Cairo University
Investigators
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Study Director: Mushira M Dahba, Doctorate Cairo University

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Responsible Party: Marina Salib, Masters degree student, Cairo University
ClinicalTrials.gov Identifier: NCT03726970     History of Changes
Other Study ID Numbers: RAD
First Posted: November 1, 2018    Key Record Dates
Last Update Posted: April 24, 2019
Last Verified: October 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No