- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07683910
Sequential PVP-I and FV
Sequential Application of PVP-I and Fluoride Varnish: A Prospective Cohort Study
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Primary Objectives:
- 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.
- 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:
- Previous treatment with fluoride varnish
- Known allergy to iodine
- Diagnosis of thyroid disease
- Chronic, prophylactic use of antibiotics
- Treatment with another investigational drug or other intervention within 30 days preceding the Baseline Visit.
- Visible cavities (d2-4) in the erupted primary teeth
- Presence of intraoral soft tissue pathology (gum boil)
- 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.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Peter Milgrom, DDS
- Telefonnummer: 206-251-6831
- E-mail: drmilgrom@silverarrest.com
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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:
- Previous treatment with fluoride varnish
- Known allergy to iodine
- Diagnosis of thyroid disease
- Chronic, prophylactic use of antibiotics
- Treatment with another investigational drug or other intervention within 30 days preceding the Baseline Visit.
- Visible cavities (d2-4) in the erupted primary teeth
- Presence of intraoral soft tissue pathology (gum boil)
- Parent anticipates the child will move from current city during the next 24 months.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Povi+Fluorimax
Topical 10% Povidone Iodine followed by Fluorimax Fluoride Varnish Applied to the Teeth
|
sodium fluoride, 2.5%
Povidone Iodine, 10%
|
|
Placebo+Fluorimax
Topical Placebo followed by Fluorimax Fluoride Varnish Applied to the Teeth
|
sodium fluoride, 2.5%
|
|
Placebo+ClinPro
Topical Placebo followed by ClinPro Clear Fluoride Applied to the Teeth
|
sodium fluoride, 2.1%
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Surface level caries
Tidsramme: 24 months
|
d2-4mfs
|
24 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Presence/Absence of dental caries lesions
Tidsramme: 24 months
|
d2-4mfs>0
|
24 months
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Tania Caceres Padilla, DDS, Universidad Nacional del Altiplano de Puno
Publikationer og nyttige links
Generelle publikationer
- 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.
- 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.
- 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.
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Stomatognatiske sygdomme
- Tandsygdomme
- Tand demineralisering
- Caries i tænderne
- Organiske kemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Alkener
- Kulbrinter, acyklisk
- Kulbrinter
- Uorganiske kemikalier
- Polymerer
- Makromolekylære stoffer
- Biomedicinske og tandmaterialer
- Fremstillede materialer
- Teknologi, industri og landbrug
- Pyrrolidiner
- Plast
- Pyrrolidinoner
- Jodforbindelser
- Iodaforer
- Polyvinyler
- Vinylforbindelser
- Povidon
- Povidon-jod
Andre undersøgelses-id-numre
- Povi 2026-1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
produkt fremstillet i og eksporteret fra U.S.A.
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .