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Sequential PVP-I and FV

Sequential Application of PVP-I and Fluoride Varnish: A Prospective Cohort Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07683910
Enrollment
393
Registered
2026-07-06
Start date
2026-09-01
Completion date
2029-03-01
Last updated
2026-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries

Keywords

Early Childhood Caries, Fluoride Varnish, Povidone-Iodine

Brief summary

This prospective cohort study in children will determine if: topical povidone iodine 10% followed by topical fluoride varnish is superior to placebo iodine followed two different varnishes alone to prevent tooth decay (dental caries).

Detailed description

Primary Objectives: 1. To determine if sequential topical application of Povidone Iodine (Povi-One, 10% PVP-I) followed by the Fluoride Varnish (Fluorimax, 2.5% NaF) every 3 months is superior to an active control (placebo + standard of care FV (Fluorimax) at 24 months post baseline. Specifically, prevention of caries lesions in primary teeth that either are sound, have only d1 (white spots) lesions or unerupted at baseline. 2. To determine if the sequential topical application of Povidone Iodine (Povi-One, 10% PVP-I) followed by the Fluoride Varnish (Fluorimax, 2.5% NaF) every 3 months is superior to active control (placebo + ClinPro Clear Fluoride Treatment (Solventum, 2.1% NaF) at 24 months post baseline. Specifically, prevention of caries lesions in primary teeth that either are sound, have only d1 (white spots) lesions or unerupted at baseline. Secondary Objective: To determine if sequential topical application of placebo followed by the Fluoride Varnish (Fluorimax, 2.5% NaF) every 3 months is superior to placebo followed by Clinpro Clear Fluoride Treatment (Solventum, 2.1% NaF) at 24 months post baseline. Study Design: Open label prospective cohort study. The study will be conducted in two hospitals in Puno serving the "Control de Crecimiento y Desarrollo (CRED)" program, conducted under the Ministry of Health. The treatment at each site will be the same with different treatments on different days of the week chosen randomly, stratified by hospital. There will be no individual randomization. Participants: Children 6-24 months of age at enrollment. To be eligible a child will have at least 1 erupted tooth that is either sound or has only a d1 (white spot) lesion. Children will be excluded under the following conditions: 1. Previous treatment with fluoride varnish 2. Known allergy to iodine 3. Diagnosis of thyroid disease 4. Chronic, prophylactic use of antibiotics 5. Treatment with another investigational drug or other intervention within 30 days preceding the Baseline Visit. 6. Visible cavities (d2-4) in the erupted primary teeth 7. Presence of intraoral soft tissue pathology (gum boil) 8. Parent anticipates the child will move from current city during the next 24 months. Products Being Studied: The 10% PVP-I (Povi-One) and 2.5% FV (Fluorimax) will be obtained from Elevate Oral Care, LLC., West Palm Beach, FL USA. The ClinPro Clear (2.1% NaF) will be purchased in the marketplace by Elevate and made available to the study.

Interventions

DEVICEfluoride varnish, 2.5%

sodium fluoride, 2.5%

DEVICEtopical fluoride, 2.1%

sodium fluoride, 2.1%

Povidone Iodine, 10%

Sponsors

Advantage Silver Dental Arrest, LLC
Lead SponsorINDUSTRY
Universidad Nacional del Altiplano de Puno
CollaboratorUNKNOWN
University of Washington
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Months to 24 Months
Healthy volunteers
Yes

Inclusion criteria

* Children 6-24 months of age at enrollment. To be eligible a child will have at least 1 erupted tooth that is either sound or has only a d1 (white spot) lesion.

Exclusion criteria

1. Previous treatment with fluoride varnish 2. Known allergy to iodine 3. Diagnosis of thyroid disease 4. Chronic, prophylactic use of antibiotics 5. Treatment with another investigational drug or other intervention within 30 days preceding the Baseline Visit. 6. Visible cavities (d2-4) in the erupted primary teeth 7. Presence of intraoral soft tissue pathology (gum boil) 8. Parent anticipates the child will move from current city during the next 24 months.

Design outcomes

Primary

MeasureTime frameDescription
Surface level caries24 monthsd2-4mfs

Secondary

MeasureTime frameDescription
Presence/Absence of dental caries lesions24 monthsd2-4mfs\>0

Contacts

CONTACTPeter Milgrom, DDS
drmilgrom@silverarrest.com206-251-6831
PRINCIPAL_INVESTIGATORTania Caceres Padilla, DDS

Universidad Nacional del Altiplano de Puno

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 7, 2026