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Immediate Implant Placement With Immediate Professionalization in Aesthetic Area

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ClinicalTrials.gov Identifier: NCT03665025
Recruitment Status : Not yet recruiting
First Posted : September 11, 2018
Last Update Posted : September 11, 2018
Sponsor:
Information provided by (Responsible Party):
mohammed nashmi hammad, Cairo University

Brief Summary:
Immediate implant placement with immediate professionalization in the maxillary esthetic zone using mixture of allograft and xenograft vs xenografts to augment the jumping gap

Condition or disease Intervention/treatment Phase
Implant Site Reaction Other: immediate implant using mixed allograft and xenograft Not Applicable

Detailed Description:
Implant placement in fresh extraction sockets in conjunction with appropriate guided bone regeneration has many benefits, which ultimately affect the total treatment plan. The immediate placement of implants provides significant advantages, including fewer surgical procedures, shorter treatment time, and improved esthetics. The goals of osseous replacement are maintenance of contour, elimination of dead space, and reduce postoperative infection, provide good support for dental implant and enhance bony and soft tissue healing. allograft bone has gold standard over other augment techniques including favorable bone quality and minimal bone resorption.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 2 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: jumping gap area in aesthetic area
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Immediate Implant Placement With Immediate Professionalization in the Maxillary Esthetic Zone Using Mixture of Allograft and Xenograft vs Xenografts to Augment the Jumping Gap
Estimated Study Start Date : January 1, 2019
Estimated Primary Completion Date : January 1, 2019
Estimated Study Completion Date : January 1, 2019

Arm Intervention/treatment
Experimental: immediate implant placement with xenograft
Immediate implant placement with the use of xenograft as grafting material
Other: immediate implant using mixed allograft and xenograft
immediate implant using mixed allograft and xenograft in anterior area to fill jumping area

Experimental: immediate implant using mixed allograft and xenograft
Immediate implant placement with using mixture of allograft and xenograft material
Other: immediate implant using mixed allograft and xenograft
immediate implant using mixed allograft and xenograft in anterior area to fill jumping area




Primary Outcome Measures :
  1. Crestal bone loss [ Time Frame: 1 year ]
    Will be measured using calliper with scale(1-10mm) for evaluation of crestal bone loss around implant which are the lower values represent a better outcome.


Secondary Outcome Measures :
  1. Patient satisfaction [ Time Frame: 1 year ]
    Will be measured using a satisfaction table chart which divided in 4 paraments with scale from 1-4 include( pain-infection-radiography-successful implant ),the number represent (4 excellent-3 very good -2 good-1 bad)



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Ages Eligible for Study:   20 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Adult patients with badly broken teeth in upper esthetic zone indicated for extraction, presence of at least 4 mm of bone beyond the root apex to guarantee implant primary stability, implant placement within the alveoli confines.
  • Both sexes.
  • No intraoral soft and hard tissue pathology.
  • No systemic condition that contraindicate implant placement.

Exclusion Criteria:

  • Presence of fenestrations or dehiscence of the residual bony Walls after extraction.
  • Heavy smokers more than 20 cigarettes per day .(24)
  • Patients with systemic disease that may affect normal healing.
  • Psychiatric problems
  • Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site.

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): NCT03665025


Contacts
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Contact: mohamed hammad, BDS 0096551553531 dr_nucler@hotmail.com

Locations
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Kuwait
Mohammed Terminated
Kuwait, Q8, Kuwait, 00965
Sponsors and Collaborators
Cairo University

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Responsible Party: mohammed nashmi hammad, Lecturer of oral and maxillofacial surgery-Cairo university, Cairo University
ClinicalTrials.gov Identifier: NCT03665025     History of Changes
Other Study ID Numbers: 14422017463550
First Posted: September 11, 2018    Key Record Dates
Last Update Posted: September 11, 2018
Last Verified: September 2018

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