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Bone Density in Immediate Implant Placment and Loading(BDIIPL)

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ClinicalTrials.gov Identifier: NCT03626779
Recruitment Status : Unknown
Verified August 2018 by Ahmed adel shaaban, Cairo University.
Recruitment status was:  Not yet recruiting
First Posted : August 13, 2018
Last Update Posted : August 22, 2018
Sponsor:
Information provided by (Responsible Party):
Ahmed adel shaaban, Cairo University

Study Description
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Brief Summary:
Atrumatic extraction ,immediate implant placment , prf as plug,immediate loading , mesure bone density 0-3-6-9 month

Condition or disease Intervention/treatment Phase
Bone Density Increased Other: Prf Not Applicable

Detailed Description:
Atrumatic extraction unrestorable tooth in esthetic zone and immediate implant placment and withdrow 10cc blood sample to gain prf plug as membrane and immediate provisional for one week and final restoration after 1 week , and mesure bone density from 0-3-6-9 month
Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 10 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
Official Title: Prf Controlled,Randamized Cinical Trial of EFFECTS OF THE PLATELET-RICH FIBRIN (PRF) ON BONE DENSITY IN IMMEDIATE IMPLANT PLACEMENT AND LOADING IN ESTHETIC ZONE
Estimated Study Start Date : September 1, 2018
Estimated Primary Completion Date : August 30, 2019
Estimated Study Completion Date : August 30, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Bone Density

Arms and Interventions
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Arm Intervention/treatment
immediate placment and loading with prf
Immediat placment and loading with prf
 Other: Prf
Take 10cc blood from patient and gain prf blug
No Intervention: immediate implant placment and loading
Immediate implant placment and loading without prf


Outcome Measures
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Primary Outcome Measures :
  1. Bone density enhancement with prf in immediate implant placment and loding [ Time Frame: 9 month ]
    Cbct


Eligibility Criteria
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Ages Eligible for Study:   20 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion criteria:

  • unrestorable anterior tooth.
  • Good oral hygine
  • Adequate bone hieght apical to the alveolus of failing tooth to ensure primary stability .

Exclusion Criteria:

  • systematic disease which affect osteointgration.
  • Bad oral hygiene
  • Broxism, clenching, deep bite, edge to edge and abnormal habits.
  • Non-treated peeiodontal diseases.
  • Pregnancy and smokers. Severe infection. Loss of labial crest after extraction of failing tooth.
Contacts and Locations
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No Contacts or Locations Provided
More Information
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Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
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Responsible Party: Ahmed adel shaaban, CairoU, Cairo University
ClinicalTrials.gov Identifier: NCT03626779    
Other Study ID Numbers: Cairo U
First Posted: August 13, 2018    Key Record Dates
Last Update Posted: August 22, 2018
Last Verified: August 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Osteosclerosis
Osteochondrodysplasias
Bone Diseases, Developmental
Bone Diseases
Musculoskeletal Diseases