Prophylactic Effect of a CANDIDA Mouthwash, Containing the Curolox™ Peptide
Primary Purpose
Erosion of Teeth, Unspecified
Status
Withdrawn
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Candida Mouthwash with Curolox™ Peptide
Sponsored by
About this trial
This is an interventional prevention trial for Erosion of Teeth, Unspecified
Eligibility Criteria
Inclusion Criteria:
- Willing and able to understand and to follow the study procedures and instructions
- Willing to wear a dental appliance for 7 days
- Willing and able to attend the on-study visits
- Good oral hygiene throughout the study
- Written informed consent before participation in the study
Exclusion Criteria:
- Volunteer with an active periodontal disease or periodontal surgery < 1 year prior to study participation
- Volunteer with hypersensitive teeth or with any other (painful) oral pathology or defect
- Volunteer with an orthodontic appliance
- Volunteer undergoing a medical treatment
- Volunteer who is allergic to dental products
- Pregnant and lactating woman
- Concurrent participation in another clinical trial
Sites / Locations
- Aeskulap Klinik
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Candida Mouthwash with Curolox™ Peptide
Arm Description
Repeated applications 2.5 ml or 5 ml twice daily
Outcomes
Primary Outcome Measures
Detection of Curolox peptide by mass spectroscopy
The primary outcome is the detection of the Curolox™ peptide on the bovine enamel sample immediately after rinsing with the peptide-containing mouth wash by mass spectroscopy
Secondary Outcome Measures
Detection of Curolox peptide by mass spectroscopy
The secondary outcome is the detection of the Curolox™ peptide on the bovine enamel sample 12 hours, 24 hours, 48 hours and 96 hours after rinsing with the peptide-containing mouth wash by mass spectroscopy
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02308436
Brief Title
Prophylactic Effect of a CANDIDA Mouthwash, Containing the Curolox™ Peptide
Official Title
Prophylactic Effect of a CANDIDA Mouthwash, Containing the Curolox™ Peptide: a Mono-centre, Not-controlled. Not Blinded, Not-randmised in Situ Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2015
Overall Recruitment Status
Withdrawn
Why Stopped
Study is not realised.
Study Start Date
February 2015 (undefined)
Primary Completion Date
March 2015 (Anticipated)
Study Completion Date
March 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mibelle AG
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In vitro results showed a protective effect against acids for the mouthwash containing Curolox™ peptide. The goal of this in situ study is to detect the Curolox™ peptide under natural oral conditions on the tooth surface and to proof the in vitro results obtained. So far there are no effect and safety data of the Curolox™ mouthwash under natural oral conditions available.
Detailed Description
The primary objective of the study is the detection of the Curolox™ peptide on the bovine enamel sample (proof-of-concept) under in vivo conditions after rinsing with the peptide-containing mouth wash.
Secondary Objectives
The secondary objectives of the study are:
safety and tolerance of the mouthwash in participants
identification of the duration the Curolox™ peptide is present on the bovine tooth surface under in vivo conditions
identification of the most effective mouthwash rinsing volume (2.5 mL or 5 mL)
prophylactic effect of multiple applications of the mouthwash confirmation of the prophylactic effect of the Curolox™ peptide obtained in in vitro study
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erosion of Teeth, Unspecified
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Candida Mouthwash with Curolox™ Peptide
Arm Type
Experimental
Arm Description
Repeated applications 2.5 ml or 5 ml twice daily
Intervention Type
Device
Intervention Name(s)
Candida Mouthwash with Curolox™ Peptide
Other Intervention Name(s)
Candida Protect
Intervention Description
Prophylaxis - protection and care of teeth against caries & acidic challenges
Primary Outcome Measure Information:
Title
Detection of Curolox peptide by mass spectroscopy
Description
The primary outcome is the detection of the Curolox™ peptide on the bovine enamel sample immediately after rinsing with the peptide-containing mouth wash by mass spectroscopy
Time Frame
Immediately after rinsing with the mouthwash
Secondary Outcome Measure Information:
Title
Detection of Curolox peptide by mass spectroscopy
Description
The secondary outcome is the detection of the Curolox™ peptide on the bovine enamel sample 12 hours, 24 hours, 48 hours and 96 hours after rinsing with the peptide-containing mouth wash by mass spectroscopy
Time Frame
12 hours, 24 hours, 48 hours, 96 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Willing and able to understand and to follow the study procedures and instructions
Willing to wear a dental appliance for 7 days
Willing and able to attend the on-study visits
Good oral hygiene throughout the study
Written informed consent before participation in the study
Exclusion Criteria:
Volunteer with an active periodontal disease or periodontal surgery < 1 year prior to study participation
Volunteer with hypersensitive teeth or with any other (painful) oral pathology or defect
Volunteer with an orthodontic appliance
Volunteer undergoing a medical treatment
Volunteer who is allergic to dental products
Pregnant and lactating woman
Concurrent participation in another clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Besimo, Dr.med.dent.
Organizational Affiliation
Aeskulap Klinik
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ulrich P. Saxer, Dr.med.dent.
Organizational Affiliation
Aeskulap Klinik / PZZN
Official's Role
Study Director
Facility Information:
Facility Name
Aeskulap Klinik
City
Brunnen
Country
Switzerland
12. IPD Sharing Statement
Learn more about this trial
Prophylactic Effect of a CANDIDA Mouthwash, Containing the Curolox™ Peptide
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