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Effect of xylitol in treatment of post-orthodontic white spot lesions

Treatment of post-orthodontic white spot lesions with 10% xylitol varnish: A randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180913041032N2
Enrollment
84
Registered
2021-12-03
Start date
2021-12-11
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

White spot lesions. Dental caries on smooth surface limited to enamel

Interventions

Intervention 1: Intervention1: 5% fluoride varnish: Ariadent fluoride varnish (Asia ChemiTeb Co, Tehran, Iran). At the time of debonding, remaining composite material on the enamel surfaces will be re

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 25 Years

Inclusion criteria

Inclusion criteria: The subjects will be chosen within patients aged between 14 and 25 years old who had completed fixed appliance orthodontic therapy recently. Have at least one WSL on the facial surface of eight maxillary anterior teeth that was not presented before orthodontic treatment.

Exclusion criteria

Exclusion criteria: Patient’s unwillingness to be randomly assigned to one of the three treatment groups Ongoing medication for a chronic disease Chronic conditions such as asthma and allergy Any abnormal oral, medical, mental condition or neuropsychiatric disorders Regular use of oral antiseptics Any WSLs present on qualifying teeth with frank cavitation, Extensive restorations on the facial surfaces of the study teeth Dental morphologic, anatomical or developmental anomalies Alterations of the enamel, e.g. hypoplasia, fluorosis Chronic use of medication causing a dry mouth or known xerostomia Known pregnancy or breastfeeding during the course of the study Professional administration or home use of highly concentrated fluoride products not related to the study during the whole study

Design outcomes

Primary

MeasureTime frame
Enamel mineral content. Timepoint: Baseline, 6 and 12 month post orthodontic treatment. Method of measurement: DIAGNOdent pen.

Secondary

MeasureTime frame
Visual assessment of white spot lesions. Timepoint: baseline and 12 month post orthodontic treatment. Method of measurement: The labial surface of maxillary incisors, cuspids and premolars will be assessed according to Gorlick et al. score 1: no white spot lesion, score 2: slight white spot lesion (thin rim). score 3: excessive white spot lesion (thick band), and score 4: white spot lesion with cavitation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHooman Zarif Najafi

Shiraz University of Medical Sciences

zarifhooman@gmail.com+98 71 3626 3193

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026