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Remineralization Potential of Pearl Powder Compared to CPP-ACP on Enamel White Spot Lesions

Remineralization Potential of Pearl Powder Compared to CPP-ACP on Enamel White Spot Lesions (Randomized Controlled Trial)

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03976583
Enrollment
62
Registered
2019-06-06
Start date
2019-09-01
Completion date
2021-09-01
Last updated
2019-06-07

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

Conditions

White Spot Lesion

Brief summary

The aim of this study is to evaluate the remineralization potential of pearl powder on early ('white spot') lesions in enamel in orthodontic patients compared to casein phosphopeptide-amorphous calcium phosphate.

Detailed description

The aim of this study is to evaluate the remineralization potential of pearl powder on early ('white spot') lesions in enamel in orthodontic patients compared to casein phosphopeptide-amorphous calcium phosphate. The remineralisation potential will be assessed both visually and by standardised photographic image analysis. the follow up will be up to 12 months.

Interventions

Remineralising agent

Natural product

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Males or females. * Age: 12-25 years old. * Patients with good oral hygiene. * Co-operative patients who show interest to participate in the study.

Exclusion criteria

* Patients with bad oral hygiene. * Lack of patient's approval and compliance. * Presence of abnormal oral, medical, or mental condition. * Patients who are allergic to milk products. * Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frameDescription
Clinical index used for visual evaluation of white spot lesions12 monthsScores(0-No visible colour change, 1-Slight white colour change, only visible after air-drying, 2-Slight colour change with certain marked white areas, 3-White consistent colour change, 4-Distinct white colour change)

Secondary

MeasureTime frameDescription
Digital photographic image analysis12 monthsComputerised software to analyse the change in the lesion

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026