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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03391180
Other study ID # FGR/2018/45
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 26, 2017
Last updated January 4, 2018
Start date February 2018
Est. completion date July 2018

Study information

Verified date January 2018
Source Riyadh Colleges of Dentistry and Pharmacy
Contact Omar H AlKadhi, BDS, MS
Phone 966505154754
Email omar.alkadhi@riyadh.edu.sa
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the effect of ICON on White spot lesions compared to CPP-ACPF plus.


Description:

The participants were categorized to either group (group1) receiving ICON treatment method (Icon, DMG, Germany), or (group 2) who shall be receiving CPP-ACPF treatment method (Tooth Mousse plus).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date July 2018
Est. primary completion date April 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria:

- permanent dentition, in good general health and without systemic diseases, who had received fixed orthodontic treatment.

Exclusion Criteria:

- Patients with primary dentition, enamel hypoplasia, dental fluorosis or tetracycline pigmentation and carious cavity were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
ICON Remineralization
A material used for the Remineralization of white spot lesions.
CPP-ACPF
Casein phosphopeptide-Amorphous calcium phosphate fluoride used for the remineralization of white spot lesions.

Locations

Country Name City State
Saudi Arabia Riyadh Colleges of Dentistry and Pharmacy Riyadh ArRiyadh

Sponsors (1)

Lead Sponsor Collaborator
Riyadh Colleges of Dentistry and Pharmacy

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Remineralization Using DIAGNOdent Laser device. 3 Months
See also
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