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The Effects of Chlorhexidine/Thymol Varnish on Partial Denture Patient

Primary Purpose

Periodontal Disease, Caries

Status
Withdrawn
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Chlorhexidine/Thymol varnish
Sponsored by
Rosa Moreno Lopez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Periodontal Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients that are going to have a new denture fitted at the Dental School of the University of Aberdeen and Penninsula Dental School.
  • Patients aged 18 years or over.

Exclusion Criteria:

  • Patients that already have a denture.
  • Patients that are taking antibiotics.
  • Patients allergic to any of the components of the products.
  • Pregnant women.
  • Severe systemic illness.
  • Patient with active periodontal disease (BoP and pockets ≥3mm) on abutment teeth.
  • Presence of caries on abutment teeth.

Sites / Locations

  • University of Aberdeen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Chlorhexidine/Thymol varnish

Placebo varnish

Arm Description

Participants to the study will receive an application of either the placebo or the product being studied every 3 months. This will be applied on all abutment teeth using a microbrush by "painting" it over the surfaces of these teeth.

Participants to the study will receive an application of either the placebo or the product being studied every 3 months. This will be applied on all abutment teeth using a microbrush and "painting" it on all the surfaces of these teeth..

Outcomes

Primary Outcome Measures

Assess if the topical application of CHX/thymol varnish every three months on partial denture abutment teeth results in a clinicallu significant decrease in any loss of attachment compared to no application
we will measure the Loss of Attachment (LoA) around each abutment tooth at 6 points

Secondary Outcome Measures

Assess if the topical application of CHX/thymol vanirhs every three months on partial denture abutment teeth results in a clinically significant decrease in carious lesion development or progression compared to no application
We will record the presence of dental caries using ICDAS

Full Information

First Posted
July 24, 2014
Last Updated
May 12, 2017
Sponsor
Rosa Moreno Lopez
Collaborators
Ivoclar Vivadent AG
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1. Study Identification

Unique Protocol Identification Number
NCT02202304
Brief Title
The Effects of Chlorhexidine/Thymol Varnish on Partial Denture Patient
Official Title
The Effects of Chlorhexidine/Thymol Varnish on the Abutment Teeth in Partial Denture Wearers.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Researcher changed jobs. Unable to carry out the project
Study Start Date
September 10, 2017 (Anticipated)
Primary Completion Date
September 10, 2019 (Anticipated)
Study Completion Date
December 10, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rosa Moreno Lopez
Collaborators
Ivoclar Vivadent AG

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cervitec, a chlorhexidine based varnished has been proven to reduce caries risk in younger populations. This study wants to investigate if the use of this product would reduce the risk of losing abutment teeth on patients that are wearing partial dentures as the literature has proven that these teeth are more prone to caries and periodontal disease. The primary objectives of this research project are to: Assess if the topical application of CHX/thymol varnish every three months on partial denture abutment teeth results in a clinicallu significant decrease in any loss of attachment compared to no application, and Assess if the topical application of CHX/thymol vanirhs every three months on partial denture abutment teeth results in a clinically significant decrease in carious lesion development or progression compared to no application. The secondary objectives of this research project are to: 1. Assess of the topical application of CHX/thymol varnish every three months on partial denture abutment teeth compared to no application results in a clinically significant difference in: Bleeding on probing (BoP). Plaque formation. Periodontal pocket depths. Microbial composition and GCF cytokine profile of the sub gingival environment. The patients self perception of oral health.
Detailed Description
2 baseline samples of the Gingival Crevicular Fluid (GCF) and the subgingival samples. The first baseline sample will be done on the day of the first impressions and the second one the day of denture fitting. The following information will be recorded on the CRFs: Silness and Löe Plaque index, BoP, probing depth, clinical attachment level, LoA, Kennedy classification, material of the partial denture and type of clasp (or no clasp) and ICDAS code. The patient will also fill in the OHIP-14 questionnaire (Oral Health Impact Profile) to assess their self perception of oral health. A photograph of the abutment teeth and the partial denture will be taken. We will also take a full history of the patient including: name, DOB and medications. The GCF and subgingival sampled will be taken every 6 months on the appointment where the varnish is applied. All the laboratory samples will be labelles with the same identification number that the patient has been allocated and a date will also be written on it. All the samples will be analysed in Plymouth and stored in a - 50°C freezer (the samples taken at the University of Aberdeen will be stored in the same type of freezer and shipped periodically to the Penninsula University for tests maintaining the same temperature conditions). They will be testing the microbial composition and GCF cytokine profile of the sub gingival environment All measurements will be reassessed at 12 months and 24 months. In addition to the denture hygiene index: Budtz-Jørgensen (1977) Index (plaque accumulation on the denture). The data will be collected by one clinician in each dental school. All clinicians will be calibrated appropriately. Calibration: Before any examination starts we will assess the consistency of each examiner (intra-exmainer) and also the variation between exmainers (inter-exmainer reproducibility). Each examiner will independently examiner the same group of 20 subjects and compare his or her findings. When findings contain major discrepancies, subjects should be recalled in order that differences in diagnoses can be reviewed by the exmainers and resolved by group discussion. If certain examiners consistently produce significantly different results from the majority, and attmepts to correct their performance fail, they will be excluded from the team. It will be made clear to all potential examiners, before these exmainations begin, that ability to standardize examination results is not a measure of clinical skills (Oral Health Surveys 4th edition. WHO. Geneva 1997) All the data will be recorded on the case report forms (CRFs).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontal Disease, Caries

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Chlorhexidine/Thymol varnish
Arm Type
Experimental
Arm Description
Participants to the study will receive an application of either the placebo or the product being studied every 3 months. This will be applied on all abutment teeth using a microbrush by "painting" it over the surfaces of these teeth.
Arm Title
Placebo varnish
Arm Type
Placebo Comparator
Arm Description
Participants to the study will receive an application of either the placebo or the product being studied every 3 months. This will be applied on all abutment teeth using a microbrush and "painting" it on all the surfaces of these teeth..
Intervention Type
Drug
Intervention Name(s)
Chlorhexidine/Thymol varnish
Other Intervention Name(s)
Cervitec Plus (1% chlorhexidine plus 1% thymol)
Intervention Description
This will be applied on abutment teeth on partial denture wearers every 3 months during a period of 2 years.
Primary Outcome Measure Information:
Title
Assess if the topical application of CHX/thymol varnish every three months on partial denture abutment teeth results in a clinicallu significant decrease in any loss of attachment compared to no application
Description
we will measure the Loss of Attachment (LoA) around each abutment tooth at 6 points
Time Frame
Assesed at the begining, at 12 months and at 24 months
Secondary Outcome Measure Information:
Title
Assess if the topical application of CHX/thymol vanirhs every three months on partial denture abutment teeth results in a clinically significant decrease in carious lesion development or progression compared to no application
Description
We will record the presence of dental caries using ICDAS
Time Frame
at the beginning, at 12 months and at 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients that are going to have a new denture fitted at the Dental School of the University of Aberdeen and Penninsula Dental School. Patients aged 18 years or over. Exclusion Criteria: Patients that already have a denture. Patients that are taking antibiotics. Patients allergic to any of the components of the products. Pregnant women. Severe systemic illness. Patient with active periodontal disease (BoP and pockets ≥3mm) on abutment teeth. Presence of caries on abutment teeth.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rosa Moreno Lopez, BDS
Organizational Affiliation
University of Aberdeen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Aberdeen
City
Aberdeen
State/Province
Aberdeenshire
ZIP/Postal Code
AB252ZR
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
within 6 months
Citations:
PubMed Identifier
19497653
Citation
Baca P, Clavero J, Baca AP, Gonzalez-Rodriguez MP, Bravo M, Valderrama MJ. Effect of chlorhexidine-thymol varnish on root caries in a geriatric population: a randomized double-blind clinical trial. J Dent. 2009 Sep;37(9):679-85. doi: 10.1016/j.jdent.2009.05.001. Epub 2009 May 13.
Results Reference
background
PubMed Identifier
19318078
Citation
Tanaka J, Tanaka M, Kawazoe T. Longitudinal research on the oral environment of elderly wearing fixed or removable prostheses. J Prosthodont Res. 2009 Apr;53(2):83-8. doi: 10.1016/j.jpor.2008.10.003. Epub 2009 Jan 10.
Results Reference
background
PubMed Identifier
19818702
Citation
Shimura Y, Wadachi J, Nakamura T, Mizutani H, Igarashi Y. Influence of removable partial dentures on the formation of dental plaque on abutment teeth. J Prosthodont Res. 2010 Jan;54(1):29-35. doi: 10.1016/j.jpor.2009.08.003. Epub 2009 Oct 8.
Results Reference
background
PubMed Identifier
16433641
Citation
Clavero J, Baca P, Paloma Gonzalez M, Valderrama MJ. Efficacy of chlorhexidine-thymol varnish (Cervitec) against plaque accumulation and gingival inflammation in a geriatric population. Gerodontology. 2006 Mar;23(1):43-7. doi: 10.1111/j.1741-2358.2006.00085.x.
Results Reference
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The Effects of Chlorhexidine/Thymol Varnish on Partial Denture Patient

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