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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03963791
Other study ID # Oper_607
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 5, 2019
Est. completion date June 1, 2020

Study information

Verified date May 2019
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research is conducted to compare the remineralization efficacy of eggshell powder gel and CPP-ACP (MI paste) on post-orthodontic white spot lesions.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date June 1, 2020
Est. primary completion date April 5, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 13 Years to 35 Years
Eligibility Inclusion Criteria:

- A patient who has just completed a comprehensive orthodontic treatment.

- Presence of at least one WSL, DIAGNOdent score (0-20).

- Age range between 13 and 35years.

Exclusion Criteria:

- Patients are unable to return for recall appointments.

- High caries risk.

- Have plaque accumulation and a periodontal problem

- In progress treatment of chronic disease.

- Presence of abnormal oral, medical, or mental condition (including any milk-related allergies or any medical condition involving kidneys or salivary glands).

- Presence of dentin caries, enamel hypoplasia or restorations on maxillary anterior teeth.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Eggshell powder gel
Eggshell powder gel produced from chicken eggs.
CPP-ACP crème
A water-based, sugar-free topical cream containing Recaladent (CCP-ACP) which is derived from the milk protein.

Locations

Country Name City State
Egypt Cairo univercity Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary white spot lesion progression. The change in the lesion fluorescence will be evaluated using diode laser fluorescence device (Diagnodent). 6 months.
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