A Prospective, Randomized Clinical Study on the Effects of Casein Phosphopeptide-amorphous Calcium Phosphate (CPP-ACP) Paste on Plaque, Gingivitis and White Spot Lesions in Orthodontic Patients - Part 2
This study is currently recruiting participants.
Verified February 2013 by University Hospital, Ghent
Sponsor:
University Hospital, Ghent
Collaborator:
GC Europe, Belgium
Information provided by (Responsible Party):
University Hospital, Ghent
ClinicalTrials.gov Identifier:
NCT00670618
First received: April 30, 2008
Last updated: February 1, 2013
Last verified: February 2013
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Purpose
Influence of CPP-ACP paste and Elmex Medical Gel on the prevention of white spot lesions in orthodontic patients during fixed appliances.
| Condition | Intervention |
|---|---|
|
Early Caries Lesions |
Device: CPP-ACP (GC Tooth Mousse) Device: CPP-ACP (GC MI Paste Plus) Device: Fluoride (Elmex Medical Gel) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Treatment |
| Official Title: | A Prospective, Randomized Clinical Study on the Effects of CPP-ACP Paste on Plaque, Gingivitis and White Spot Lesions in Orthodontic Patients - Part 2 |
Resource links provided by NLM:
Further study details as provided by University Hospital, Ghent:
Primary Outcome Measures:
- Prevention of the opacity of white spots during orthodontic treatment with fixed appliances [ Time Frame: After 2 years ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 400 |
| Study Start Date: | June 2008 |
| Estimated Study Completion Date: | May 2013 |
| Estimated Primary Completion Date: | May 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
CPP-ACP (GC Tooth Mousse)
|
Device: CPP-ACP (GC Tooth Mousse)
Calcium and phosphate
|
|
Experimental: 2
GCC-ACP (GC MI Paste Plus)
|
Device: CPP-ACP (GC MI Paste Plus)
Calcium, phosphate and fluoride
|
|
Experimental: 3
Fluoride (Elmex Medical Gel)
|
Device: Fluoride (Elmex Medical Gel)
Fluoride
|
|
No Intervention: 4
Control group
|
Eligibility| Ages Eligible for Study: | 10 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- No white spot lesion at the time of placement of fixed appliances
Exclusion Criteria:
- White spots already present before start orthodontic treatment
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00670618
Contacts
| Contact: Silvia Dauwe | silvia.dauwe@ugent.be |
Locations
| Belgium | |
| University Hospital Ghent | Recruiting |
| Ghent, Belgium, 9000 | |
| Principal Investigator: Guy De Pauw, MD, PhD | |
Sponsors and Collaborators
University Hospital, Ghent
GC Europe, Belgium
Investigators
| Principal Investigator: | Guy De Pauw, MD, PhD | University Hospital, Ghent |
More Information
Additional Information:
No publications provided
| Responsible Party: | University Hospital, Ghent |
| ClinicalTrials.gov Identifier: | NCT00670618 History of Changes |
| Other Study ID Numbers: | 2008/187 - Part 2 |
| Study First Received: | April 30, 2008 |
| Last Updated: | February 1, 2013 |
| Health Authority: | Belgium: Institutional Review Board |
Additional relevant MeSH terms:
|
Gingivitis Dental Caries Gingival Diseases Periodontal Diseases Mouth Diseases Stomatognathic Diseases Tooth Demineralization |
Tooth Diseases Fluorides Cariostatic Agents Protective Agents Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 23, 2013