- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00399620
Chromogranin-A-Derived Peptides and Periodontitis in Diabetic Patients
January 9, 2009 updated by: University Hospital, Strasbourg, France
Chromogranin-A-Derived Peptides in the Gingival Crevicular Fluid and the Saliva of Diabetic Patients With or Without Periodontitis
Periodontitis is a chronic disease of the supporting tissue of the teeth, characterized by bleeding and inflamed gingival, resorption of alveolar bone.
This disease has a significant impact of the quality of life as the teeth become progressively mobile and may fall out spontaneously if no treatment is provided.
Periodontal disease has been cited as the sixth complication of diabetes mellitus.Chromogranins / secretogranins are a family of proteins present in nervous endocrine and immune cells, released with catecholamines during stress situations.
Chromogranin A (CGA) is the major member of this family.The aim of this study is to determine the level of CGA and its derived peptides in the gingival crevicular fluid (GCF) of health or diabetic patients with and without periodontitis.Then, we want to determine the antimicrobial activity of these peptides.
Study Overview
Status
Unknown
Conditions
Study Type
Interventional
Enrollment (Anticipated)
90
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Strasbourg, France, 67091
- Recruiting
- Département de Parodontologie - Hôpital Civil
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Contact:
- Martine Soell, MD
- Phone Number: 33.6.74.86.67.36
- Email: martine.soell@chru-strasbourg.fr
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Principal Investigator:
- Martine Soell, MD
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Sub-Investigator:
- Frédéric Blickle, MD
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion criteria:
- Patients from 20 to 80 years old
- A minimum of 10 teeth
- Healthy volunteers or diabetic patients with or without periodontitis
Exclusion criteria:
- a course of antibiotics
- a fungicidal therapy
- a corticotherapy
- a hormone therapy
- a pregnancy
- persons under guardianship
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Martine Soell, MD, Hopitaux universitaires de Strasbourg
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2008
Study Registration Dates
First Submitted
November 14, 2006
First Submitted That Met QC Criteria
November 14, 2006
First Posted (Estimate)
November 15, 2006
Study Record Updates
Last Update Posted (Estimate)
January 12, 2009
Last Update Submitted That Met QC Criteria
January 9, 2009
Last Verified
January 1, 2009
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3739
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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