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. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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25 May 2015 |
Main ID: |
NCT02438046 |
Date of registration:
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27/04/2015 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Platelet Rich Fibrin in the Treatment of Palatal Wounds
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Scientific title:
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Platelet Rich Fibrin in the Treatment of Palatal Wounds After Epithelialized Free Gingival Grafts Harvesting. A Randomized Clinical Trial |
Date of first enrolment:
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May 2015 |
Target sample size:
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40 |
Recruitment status: |
Not yet recruiting |
URL:
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http://clinicaltrials.gov/show/NCT02438046 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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Phase:
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Phase 4
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Countries of recruitment
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Italy
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Contacts
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Name:
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Michele Paolantonio, MD; DDS |
Address:
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Telephone:
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+393395204073 |
Email:
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mpaoantonio@unich.it |
Affiliation:
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Name:
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Michele Paolantonio, MD; DDS |
Address:
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Telephone:
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+393395204073 |
Email:
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mpaolantonio@unich.it |
Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria: are as follows:
- to have a single gingival recession to be treated by a mucogingival surgery
intervention
- to be in good systemic health
- to have a good oral hygiene
Exclusion Criteria:
- no systemic diseases; no coagulation disorders; no medications affecting periodontal
status in the previous 6 months; no pregnancy or lactation;
- no smoking habits;
- no periodontal surgery on the experimental sites;
- no inadequate endodontic treatment
- no tooth mobility at the site of surgery
Age minimum:
N/A
Age maximum:
70 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Gingival Recession
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Intervention(s)
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Procedure: Palatal wound bandage
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Primary Outcome(s)
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The primary outcome is to assess the time needed to obtain a complete re epithelialization of the palatal wound
[Time Frame: four weeks]
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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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