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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT02190409 |
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Date of registration:
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08/07/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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An Invivo Study to Compare the Stability of Dental Implants With or Without Platelet Rich Fibrin Application
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Scientific title:
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The Effect Of Platelet Rich Fibrin on Implant Stability |
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Date of first enrolment:
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December 2011 |
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Target sample size:
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20 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT02190409 |
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Study type:
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Interventional |
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Study design:
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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Phase:
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N/A
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Countries of recruitment
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Turkey
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Contacts
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Name:
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ELIF ÖNCÜ, 1 |
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Address:
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Telephone:
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Email:
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Affiliation:
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NECMETTIN ERBAKAN UNIVERSITY |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- The absence of any lesions in the oral cavity, and sufficient residual bone volume to
receive two or more adjacent implants of =3.5 mm in diameter and 11.0 mm in length,
and extracted at least 6 months ago.
Exclusion Criteria:
- Insufficient bone volume
- Parafunctional habits
- Smoking more than 10 cigarettes per day
- Excessive consumption of alcohol
- Localized radiotherapy of the oral cavity
- Antitumor chemotherapy
- Liver, blood, and kidney diseases
- Immunosuppression
- Current corticosteroid or bisphosphonate use
- Pregnancy
- Mucocutaneous diseases involving oral cavity
- Poor oral hygiene
Age minimum:
18 Years
Age maximum:
55 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Dental Implant
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Intervention(s)
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Device: Dental implant
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Primary Outcome(s)
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Implant Stabilitty Quotient (ISQ) evaluation: analysis of the resonance frequency values 4 week period.
[Time Frame: Resonance frequency measurements were made by Osstell ISQ after placement of implants, at 1 week and one month postoperatively.]
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Secondary Outcome(s)
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Evaluation of osseointegration in different types of bone
[Time Frame: Resonance frequency measurements in different bone types were made by Osstell ISQ after placement of implants, at 1 week and one month postoperatively.]
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Secondary ID(s)
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D-KA11/06
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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