World Health Organization site
Skip Navigation Links

Main
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: ClinicalTrials.gov
Last refreshed on: 25 May 2015
Main ID:  NCT02438046
Date of registration: 27/04/2015
Prospective Registration: Yes
Primary sponsor: G. d'Annunzio University
Public title: Platelet Rich Fibrin in the Treatment of Palatal Wounds
Scientific title: Platelet Rich Fibrin in the Treatment of Palatal Wounds After Epithelialized Free Gingival Grafts Harvesting. A Randomized Clinical Trial
Date of first enrolment: May 2015
Target sample size: 40
Recruitment status: Not yet recruiting
URL:  http://clinicaltrials.gov/show/NCT02438046
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment  
Phase:  Phase 4
Countries of recruitment
Italy
Contacts
Name:     Michele Paolantonio, MD; DDS
Address: 
Telephone: +393395204073
Email: mpaoantonio@unich.it
Affiliation: 
Name:     Michele Paolantonio, MD; DDS
Address: 
Telephone: +393395204073
Email: mpaolantonio@unich.it
Affiliation: 
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Gingival Recession
Intervention(s)
Procedure: Palatal wound bandage
Primary Outcome(s)
The primary outcome is to assess the time needed to obtain a complete re epithelialization of the palatal wound [Time Frame: four weeks]
Secondary Outcome(s)
Secondary ID(s)
1/2015
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history