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Effect of Bioactive Resin Material Containing S-PRG Filler on White Spot Lesions

Effect of Bioactive Resin Material Containing S-PRG Filler on White Spot Lesions: A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07715942
Enrollment
50
Registered
2026-07-21
Start date
2025-07-13
Completion date
2026-12-23
Last updated
2026-07-21

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

Conditions

White Spot Lesion of Tooth

Keywords

Clear aligners, Bioactive resin, Composite containing S-PRG filler, QLF, Clear aligners, Bioactive resin, Composite containing S-PRG filler, Quantitative Light-Induced Fluorescence (QLF)

Brief summary

the effect of bioactive resin composite containing S-PRG filler will be tested as the material of choice for attachments bonded on teeth prior to the use of orthodontic clear aligners compared to the conventionally used flowable composite material for the prevention of white spot lesions on enamel tooth surfaces

Interventions

OTHERBioactive resin composite containing S-PRG filler

Bioactive resin composite containing S-PRG filler is used as attachment material for the orthodontic clear aligners

OTHERConventional flowable composite is used for the attachments for the clear orthodontic aligners

Conventional flowable composite is used for the attachments for the clear orthodontic aligners

Sponsors

Jordan University of Science and Technology
Lead SponsorOTHER
Jordan University of Science and Technology/Deanship of Scientific Research
CollaboratorUNKNOWN

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy young adult orthodontic patients * Class 1 malocclusion with mild to moderate crowding (\<6 mm). * Non extraction treatment plan. * Optimum oral Hygiene before treatment. * A maximum of three restored teeth with either fillings or prosthesis.

Exclusion criteria

* Patients with defective enamel, fluorosis, hypocalcification or enamel hypoplasia. * Extensive restorations. * Syndromes and Oro-facial anomalies. * Salivary gland diseases. * Patients who are pregnant, diabetic, or using mouth rinses or interacting medications, including antibiotic therapy.

Design outcomes

Primary

MeasureTime frameDescription
White spot lesion area6 monthsIt measures the area of enamel demineralization (in pixels) using QLF system
Mean of fluorescence loss (Delta F)6 monthsIt measures the percentage of fluorescence loss in the white spot lesion compared to that of sound reflecting the amount of mineral loss using QLF system

Countries

Jordan

Contacts

STUDY_DIRECTORSusan Al-Khateeb

Jordan University of Science and Technology

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 22, 2026