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Chlorhexidine as Coadjuvant in Dentin Adhesion of Noncarious Cervical Lesions

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ClinicalTrials.gov Identifier: NCT01947192
Recruitment Status : Completed
First Posted : September 20, 2013
Last Update Posted : February 24, 2016
Sponsor:
Information provided by (Responsible Party):
Maximiliano Sergio Cenci, Federal University of Pelotas

August 15, 2013
September 20, 2013
February 24, 2016
November 2011
November 2012   (Final data collection date for primary outcome measure)
Change from baseline in Retention rates of the restoration at 24 months [ Time Frame: 6, 12 and 24 months ]
Patients will be reevaluated at each specified time point and all restoration sites will be evaluated to check if the restoration will be still in place, or if it is missing, or if there is partial retention
Same as current
Complete list of historical versions of study NCT01947192 on ClinicalTrials.gov Archive Site
  • Change from baseline in Post-operative sensitivity at 6-month [ Time Frame: baseline and 6-month ]
    At each time-point, patients will be recalled and interviewed regarding any symptom related to each restorations placed.
  • Change from baseline in marginal staining rates at 6. 12 and 24 months [ Time Frame: 6, 12 and 24 months ]
    At each time-point, patients will be recalled and restorations will be reassessed in order to record changes in the rates of marginal staining, using the World Dental Federation (FDI) criteria for restorations assessment (Hickel et al 2010).
Same as current
Not Provided
Not Provided
 
Chlorhexidine as Coadjuvant in Dentin Adhesion of Noncarious Cervical Lesions
Chlorhexidine as Coadjuvant in Dentin Adhesion of Noncarious Cervical Lesions and Failure-prognostic Variables: A Randomized Controlled Trial

This study aims to evaluate the effect of chlorhexidine digluconate (CRX) application in etched dentin on the retention of noncarious cervical lesions restorations.

A randomized controlled split-mouth and blind trial will be carried out. Patients with at least two non-carious cervical lesions (NCL) will be selected. NCL will be randomly assigned according the type of teeth (incisors, canine or pre-molars) into two groups: control or experimental group (application of 2% CRX for 60 seconds after the acid etching procedure). Class V restorations will be performed out with an etch-and-rinse adhesive system (Adper Single Bond 2-3M ESPE) and a composite resin (Filtek Z350-3M ESPE) according the manufacture instructions, by previously trained operators. The restorations will be evaluated by a calibrate examiner at 1 week (baseline), and 6-month, 12-month and 24-month, using the World Dental Federation (FDI) criteria. The outcome is retention of the restoration.

Not Provided
Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose: Treatment
Non-carious Cervical Lesions
  • Procedure: Treatment with chlorhexidine
    Application of 2% chlorhexidine digluconate (60 seconds) after the etching procedure and before the adhesive system.
  • Procedure: Water pre-treatment
    Treatment of acid etched dentin with sterilized water for 60 s before adhesive system application
  • Experimental: Chlorhexidine
    Dentin pre-treatment with a experimental solution (chlorhexidine), after the dentin acid etching
    Intervention: Procedure: Treatment with chlorhexidine
  • Placebo Comparator: Water
    Application of water (placebo) after dentin acid etching.
    Intervention: Procedure: Water pre-treatment
Hickel R, Peschke A, Tyas M, Mjör I, Bayne S, Peters M, Hiller KA, Randall R, Vanherle G, Heintze SD. FDI World Dental Federation: clinical criteria for the evaluation of direct and indirect restorations-update and clinical examples. Clin Oral Investig. 2010 Aug;14(4):349-66. doi: 10.1007/s00784-010-0432-8. Epub 2010 Jul 14.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
Same as current
Not Provided
November 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients presenting at least two non-carious cervical lesions (NCL) in anterior, canine or pre-molars;
  • Patients who had more than 20 teeth in the mouth;
  • Patients who were at least 18 years of age at the time of treatment and capable to understand and sign the written informed consent;
  • NCL with at least 1 mm of depth in a vital permanent incisor, canine or premolar of the upper as the lower jaw.
  • NCL in the facial surface of the teeth with sometimes a small part extending interproximally;
  • Patients with good periodontal heath.

Exclusion Criteria:

  • Patients with smoking habits, practicing bruxism, severe systemic diseases, using active orthodontic treatment, malocclusion (Angle Class II or Class III);
  • Tooth with the NCL with the absent of antagonist;
  • NCL wear facets upper than 50% of the incisal/occlusion surface, as a result of tooth attrition;
  • Presence of caries or restorations in the area to be treated;
  • Full-mouth visible plaque index (VPI) or full-mouth gingival bleeding index upper than 20%, probing depth and clinical attachment loss values exceeding 4 mm with bleeding on probing;
  • Unwillingness to return for follow-ups or refuse to participate.
Sexes Eligible for Study: All
18 Years to 70 Years   (Adult, Older Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
Brazil
 
 
NCT01947192
PPGO0017
Not Provided
Not Provided
Not Provided
Maximiliano Sergio Cenci, Federal University of Pelotas
Federal University of Pelotas
Not Provided
Principal Investigator: Maximiliano Cenci, PhD School of Dentistry-UFPel
Federal University of Pelotas
February 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP