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Pre-extractive Inter-radicular Implant Bed Preparation Versus Conventional Post-extractive Inter-radicular Implant Bed Preparation in Mandibular Molars

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03640091
Recruitment Status : Unknown
Verified February 2019 by Mohamed abdel wahid elshoaby, Cairo University.
Recruitment status was:  Recruiting
First Posted : August 21, 2018
Last Update Posted : February 5, 2019
Sponsor:
Information provided by (Responsible Party):
Mohamed abdel wahid elshoaby, Cairo University

Study Description
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Brief Summary:
Pre-extractive Inter-radicular Implant Bed Preparation versus Conventional Post-extractive Inter-radicular Implant Bed Preparation in Mandibular Molars

Condition or disease Intervention/treatment Phase
Randomized Clinical Trial Procedure: Post-extractive inter-radicular implant bed preparation Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 2 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Implant in Mandibular Molars
Actual Study Start Date : August 1, 2018
Estimated Primary Completion Date : November 1, 2019
Estimated Study Completion Date : December 1, 2019
Arms and Interventions
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Arm Intervention/treatment
Experimental: Pre-extractive inter-radicular implant bed preparation Procedure: Post-extractive inter-radicular implant bed preparation
Implant placement in mandibular molars


Outcome Measures
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Primary Outcome Measures :
  1. Implant stability [ Time Frame: 1 year ]
    By ostell in newten scale


Secondary Outcome Measures :
  1. Marginal bone loss [ Time Frame: 1 year ]
    By cone beam xray in millimeters scale


Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Patients with badly decayed posterior molar teeth.
  • Distance from height of inter-radicular furcation of mandibular molars to the mandibular canal should be equal to or more than 10 mm

Exclusion Criteria:

  • Distance from height of inter-radicular furcation of mandibular molars to the mandibular canal equal to or less than 8 mm.
  • Heavy smokers more than 20 cigarettes per day.
Contacts and Locations
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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): NCT03640091


Contacts
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Contact: Mohamed Abdo Elshoaby, Responsible 01064620838 ext 0132460913 Mando_abdo_2008@yahoo.com

Locations
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Egypt
Cairo University Recruiting
Cairo, Egypt, 02
Contact: Mohamed Abdo Elshoaby, Bachelor    01064620838 ext 0132460913    Mohamedalshoaibi89@gmail.com   
Contact: Ahmed Abdo Elshoaby, Bachelor    01156989210 ext 0132475866    Mando_abdo_2008@yahoo.com   
Sponsors and Collaborators
Cairo University
More Information
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Responsible Party: Mohamed abdel wahid elshoaby, Short implant, Cairo University
ClinicalTrials.gov Identifier: NCT03640091    
Other Study ID Numbers: Cairo university 1
First Posted: August 21, 2018    Key Record Dates
Last Update Posted: February 5, 2019
Last Verified: February 2019

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