CClinicalTrials.gg
Not yet recruitingNCT07683910Updated Jul 6, 2026

Sequential PVP-I and FV

An observational study in Dental Caries, sponsored by Advantage Silver Dental Arrest, LLC. Not yet recruiting. Open to participants aged 6 Months to 24 Months, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by Advantage Silver Dental Arrest, LLC · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
393
Ages
6 Months to 24 Months
Sex
All
01

Study 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).

Read the 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.

02

Conditions studied

  • Dental Caries

Browse trials for

Keywords

  • Early Childhood Caries
  • Fluoride Varnish
  • Povidone-Iodine
03

In context

Dental Caries

1,109 studies on the registry are indexed under Dental Caries; 197 are open to participants now.

This study's planned enrollment of 393 is above the median of 180 across 177 observational studies indexed under Dental Caries.

Browse Dental Caries studies →

Lead sponsor

Advantage Silver Dental Arrest, LLC is the lead sponsor of 7 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 24 Months
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Children served by two health centers in Puno serving the "Control de Crecimiento y Desarrollo (CRED)" program and the Faculty of Health Sciences, Professional School of Dentistry, National University of the Altiplano, Puno, Peru.

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

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.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
393 participants (estimated)
Patient registry
No

Groups and cohorts

  • Povi+Fluorimax

    Topical 10% Povidone Iodine followed by Fluorimax Fluoride Varnish Applied to the Teeth

    Device: fluoride varnish, 2.5% · Drug: Povidone Iodine Topical

  • Placebo+Fluorimax

    Topical Placebo followed by Fluorimax Fluoride Varnish Applied to the Teeth

    Device: fluoride varnish, 2.5%

  • Placebo+ClinPro

    Topical Placebo followed by ClinPro Clear Fluoride Applied to the Teeth

    Device: topical fluoride, 2.1%

Interventions

  • Devicefluoride varnish, 2.5%

    sodium fluoride, 2.5%

  • Devicetopical fluoride, 2.1%

    sodium fluoride, 2.1%

  • DrugPovidone Iodine Topical

    Povidone Iodine, 10%

06

What researchers measure

Primary outcomes

  1. Surface level caries

    d2-4mfs

    Time frame: 24 months

Secondary outcomes

  1. Presence/Absence of dental caries lesions

    d2-4mfs\>0

    Time frame: 24 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Schafer JL. Analysis of Incomplete Multivariate Data. London: Chapman & Hall, 1997.
  • Warren JJ, Weber-Gasparoni K, Tinanoff N, Batliner TS, Jue B, Santo W, Garcia RI, Gansky SA; Early Childhood Caries Collaborating Centers. Examination criteria and calibration procedures for prevention trials of the Early Childhood Caries Collaborating Centers. J Public Health Dent. 2015 Fall;75(4):317-26. doi: 10.1111/jphd.12102. Epub 2015 May 22. PubMed 26011444 ↗
  • Padilla Caceres TC, Cervantes-Alagon S, Castillo JL, Vera Reyes CM, Rothen M, Mancl LA, Milgrom P. Using sequential applications of a novel silver diamine fluoride gel and sodium fluoride varnish to arrest severe early childhood caries lesions: A clinical trial with single group assignment. J Am Dent Assoc. 2024 Jun;155(6):526-535. doi: 10.1016/j.adaj.2024.02.013. Epub 2024 Apr 25. PubMed 38678451 ↗
  • Broadbent JM, Thomson WM. For debate: problems with the DMF index pertinent to dental caries data analysis. Community Dent Oral Epidemiol. 2005 Dec;33(6):400-9. doi: 10.1111/j.1600-0528.2005.00259.x. PubMed 16262607 ↗

Individual participant data

Plan to share: Yes — Deidentified participant level data will be made available upon request

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07683910
Lead sponsor
Advantage Silver Dental Arrest, LLC
Collaborators
Universidad Nacional del Altiplano de Puno, University of Washington
Responsible party
Peter Milgrom (Investigator, Advantage Silver Dental Arrest, LLC) — Principal investigator
First posted
Jul 6, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Sep 30, 2028 (estimated)
Completion
Mar 1, 2029 (estimated)
Last update
Jul 6, 2026

Study contacts

Peter Milgrom, DDS
Contact
drmilgrom@silverarrest.com
206-251-6831
Tania Caceres Padilla, DDS
principal investigator · Universidad Nacional del Altiplano de Puno

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion