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Trial record 21 of 292 for:    Sodium Fluoride OR Duraphat

Therapeutic Effect of Two Fluoride Varnishes on White Spot Lesions: a Clinical Study

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00723515
Recruitment Status : Completed
First Posted : July 28, 2008
Last Update Posted : July 28, 2008
Information provided by:
University of Pernambuco

Brief Summary:
The study hypothesis is the difference in therapeutic effect of two varnish formulations (G1 = NaF, 2.26%F, G2 = NaF, 2.71% F + CaF2). These products are commercially available in the Brazilian and international market and they are used for dental caries as white spot lesions control.

Condition or disease Intervention/treatment Phase
Dental Caries Drug: sodium fluoride Drug: sodium fluoride calcium fluoride Phase 4

Detailed Description:
The aim of this study was to evaluate the therapeutic effect of two varnish formulations (G1 = NaF, 2.26%F, G2 = NaF, 2.71% F + CaF2) on the remineralization of white spot lesions (WSL). The sample was composed of 15 (7- to 12-year-old) children with 45 active WSL in anterior permanent teeth. The children were randomly divided in two groups providing 22 lesions for G1 and 23 for G2. The children were submitted to weekly varnish applications 4 times. The WSL were evaluated twice: baseline and on week 4. Maximum lesion dimensions (mesial-distal and incisal-gingival) were measured in millimeters and classified in four grades of size. WSL were also recorded assessing lesion activity by one calibrated examiner. The Pearson chi-square and Fisher's exact tests were used (P < 0.01). WSL reductions were observed in both varnish groups (Chi-square= 0.15, d.f.=1, P=0.90); and with similar magnitude (in mm): 1.19 and 1.29 for G1 and G2, respectively. Thirty-six WLS (15 in G1 and 26 in G2) were classified as inactive in week 4 reaching an overall value of 80%. No difference was observed between G1 and G2 regarding activity scores (Fisher's exact test, p > 0.01). It can be concluded that after 4 applications the two varnish formulations tested produced similar clinical effects indicating the reduction and the control of carious activity in most WSL.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 45 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Therapeutic Effect of Two Fluoride Varnishes on White Spot Lesions: a Clinical Study
Study Start Date : February 2007
Actual Primary Completion Date : June 2007
Actual Study Completion Date : October 2007

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Rashes Tooth Decay

Arm Intervention/treatment
Active Comparator: G1
NaF (sodium fluoride varnish) with 2.26% of fluoride
Drug: sodium fluoride
sodium fluoride 5%
Other Name: Duraphat®, Colgate Palmolive GmbH, Hamburg, Germany

Experimental: G2
NaF (sodium fluoride)2.71% of fluoride plus CaF2 (calcium fluoride)
Drug: sodium fluoride calcium fluoride
sodium fluoride 5% + calcium fluoride
Other Name: Duofluorid XII®, FGM, Joinville, Brazil

Primary Outcome Measures :
  1. reduction of the size of the caries lesion [ Time Frame: 4 weeks ]

Secondary Outcome Measures :
  1. Inactivation of carious lesions [ Time Frame: 4 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   7 Years to 12 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • regular hygiene habits (brushing teeth everyday)
  • registered in public schools

Exclusion Criteria:

  • dental caries such as small cavities or restorations in the target teeth (permanent anterior teeth)
  • development enamel alterations (hypoplasia, fluorosis) or periodontal disease
  • children using orthodontic devices
  • under medical treatment
  • taking any kind of medicine
  • no informed consent form signed

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00723515

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University of Pernambuco
Camaragibe, Pernambuco, Brazil, 54753-220
Sponsors and Collaborators
University of Pernambuco
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Principal Investigator: Jainara MS Ferreira, Master University of Pernambuco
Study Chair: Ana Karla R Aragão, Graduate Univeristy of Pernambuco
Study Chair: Adriana DB Rosa, student Federal University of Paraiba
Study Chair: Fabio C Sampaio, PhD Federal Univerisity of Paraiba
Study Chair: Valdenice A Menezes, PhD Univeristy of Pernambuco

Publications automatically indexed to this study by Identifier (NCT Number):
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Responsible Party: Jainara Maria Soares Ferreira, University of Pernambuco Identifier: NCT00723515     History of Changes
Other Study ID Numbers: UPE 260/08
First Posted: July 28, 2008    Key Record Dates
Last Update Posted: July 28, 2008
Last Verified: July 2008
Keywords provided by University of Pernambuco:
White spot lesion
Tooth remineralization
Fluoride varnishes
Additional relevant MeSH terms:
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Sodium Fluoride
Fluorides, Topical
Dental Caries
Tooth Demineralization
Tooth Diseases
Stomatognathic Diseases
Calcium, Dietary
Calcium-Regulating Hormones and Agents
Physiological Effects of Drugs
Bone Density Conservation Agents
Cariostatic Agents
Protective Agents
Anti-Infective Agents, Local
Anti-Infective Agents