- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02744703
Effect of Caffeic Acid Phenethyl Ester as a Matrix Metalloproteinase Inhibitor: Randomized Controlled Clinical Trial
April 15, 2016 updated by: Prof. Dr. Mine Dundar Comlekoglu, Ege University
Professor, Ege University Faculty of Dentistry
Matrix metalloproteinases (MMPs); activated by the application of adhesive systems on dentin cause degradation of the collagen proteins and loss of bond strength in adhesive restorations.
Caffeic acid phenethyl ester (CAPE) showed inhibitory activities on dentinal MMPs.
It is hypothesised that dentin pretreatment with CAPE, as an MMP inhibitor, would be beneficial for the bonding of resin material and tooth substrate over the course of time.
This study evaluated the effect of 5 % CAPE pretreatment on the microtensile bond strength of a nanohybrid resin restoration applied with total-etch or self-etch adhesive systems on 10 patients (12-18 yrs).
Two standard cavities (3 x 3 x 4 mm) prepared on the occlusal surfaces of one of the two premolar teeth in each patient were randomly assigned into four treatment groups (n=10); 5% CAPE pretreatment and total-etch adhesive (TC), Total-etch adhesive (control) (T), 5% CAPE pretreatment and self-etch adhesive (SC), Self-etch adhesive (control) (S) followed by restoration and 3 months of intra-oral functioning.
After teeth extraction, the specimens were stored in distilled water+thymol solution at 4°C to inhibit microbial growth and used in one week period.
Dentin-composite sticks were obtained from each restoration for µTBS tests and scanning electron microscopy (SEM) evaluation.
Failure mode analysis was performed microscopically.
Data were analysed statistically using Repeated Measure ANOVA (p < 0.05).
Dentin pretreatment with CAPE solution (5%) for 60 seconds significantly increased the composite resin restorations' bond strengths to dentin applied with either total-etch or self-etch adhesive system.
Thus it can be used as an MMP inhibitor prior to the the resin restorations.
However further long term clinical studies are needed to support the use of CAPE pretreatment along with self-etch and total-etch adhesive systems.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
The aim of the present study was to evaluate the effect of caffeic acid phenethyl ester (CAPE) pretreatment used as matrix metalloproteinase (MMP) inhibitor on microtensile bond strength (µTBS) of nanohybrid resin restorations applied with total-etch or self-etch adhesive systems.
A total of 10 patients aged between 12 and 18 years old (4 males, 6 females, mean age:15) received 40 composite restorations.
The patients who had contralateral pairs of caries-free premolars which were planned to be extracted for orthodontic treatment were enrolled in the study.
This study was performed with a protocol approved by the Ethical Committee for Clinical Studies, Faculty of Medicine, University of Ege, Izmir, Turkey (04.10.2012;
no:12-8/6).
The treatments were performed after the informed consents were received both from the parents and the patients.
Included teeth were in function and no anomalies were found neither in teeth nor in occlusion.
Two standard cavities (3 x 3 x 4 mm) with continuous enamel cavosurface margins were prepared on the occlusal surfaces of each premolar tooth.Totally four cavities in each patient were randomly assigned into four treatment groups (n=10); Group TC: CAPE and total-etch adhesive (Syntac; Ivoclar Vivadent AG), Group T: Total-etch adhesive (control), Group SC: CAPE and self-etch adhesive (AdheSE; Ivoclar Vivadent AG), Group S: Self-etch adhesive (control).
All cavities were restored incrementally with a nano-filled hybrid composite resin (Tetric-N-Ceram, Ivoclar Vivadent AG) in which polymerization in each layer was performed for 40 seconds with a light-curing unit (BluePhase Ivoclar Vivadent AG) exceeding an energy output of 500mw/sec.
Study Type
Interventional
Enrollment (Actual)
10
Phase
- Not Applicable
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
12 years to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:I
- Occlusally functioning teeth without any anomalies
- Good oral hygiene
- No systemical disorders
- No periodontal diseases
- No allergic reactions to the dental materials
Exclusion Criteria:
- Patients not eligible for premolar teeth extraction for orthodontic treatment
- Poor oral hygiene
- Non-functioning premolar teeth to be included
- Patients having systemical disorders, periodontal diseases or allergic reactions to dental materials
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: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: self-etch adhesive
application of self-etch adhesive on cavities.
|
comparator use of total-etch adhesive
Other Names:
|
|
EXPERIMENTAL: CAPE-S
CAPE before self-etch adhesive
|
experimental group
Other Names:
|
|
ACTIVE_COMPARATOR: total-etch adhesive
total-etch adhesive on cavities.
|
comparator use of total-etch adhesive
Other Names:
|
|
EXPERIMENTAL: CAPE-T
CAPE before total-etch adhesive application
|
experimental group
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Determination of structural integrity of hybrid layer in forty restorations on 10 patients using scanning electron microscopy after application of different adhesive strategies and a matrix metalloproteinase inhibitor.
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
April 1, 2013
Primary Completion (ACTUAL)
April 1, 2015
Study Completion (ACTUAL)
May 1, 2015
Study Registration Dates
First Submitted
April 3, 2016
First Submitted That Met QC Criteria
April 15, 2016
First Posted (ESTIMATE)
April 20, 2016
Study Record Updates
Last Update Posted (ESTIMATE)
April 20, 2016
Last Update Submitted That Met QC Criteria
April 15, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 04.10.2012; no:12-8/6
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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