Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT07325643

Effect of Hydroxyapatite Toothpaste and Mouthwash in Preventing White Spot Lesions During Orthodontic Treatment

Led by Heba Tahseen Almasri · Updated on 2026-01-08

75

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effect of hydroxyapatite-containing toothpaste and mouthwash in preventing white spot lesions in patients undergoing orthodontic treatment. Participants: 75 patients will be divided into three groups: * Group A: Participants will brush their teeth three times a day using hydroxyapatite toothpaste and rinse twice a day with a placebo mouthwash. * Group B: Participants will brush their teeth three times a day using fluoride toothpaste and rinse twice a day with hydroxyapatite mouthwash. * Group C (Control Group): Participants will brush their teeth three times a day using fluoride toothpaste and rinse twice a day with a placebo mouthwash. Patients will be followed during their orthodontic treatment to assess the development of white spot lesions. The study is safe and involves no surgical procedures or risky medications, and will be conducted under the supervision of Principal Investigator Heba Masri after obtaining ethical approval.

CONDITIONS

Official Title

Effect of Hydroxyapatite Toothpaste and Mouthwash in Preventing White Spot Lesions During Orthodontic Treatment

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients receiving comprehensive orthodontic treatment
  • Complete permanent teeth up to first premolar with no extractions planned
  • Good overall health
  • Good oral hygiene with full-mouth plaque score less than 20%
  • No bleeding on probing after 30 seconds
  • Discontinuous band of plaque at gingival margin
  • Normal stimulated salivary flow rate
  • Normal salivary buffer capacity with final pH between 6.0 and 7.0
Not Eligible

You will not qualify if you...

  • History of previous orthodontic treatment
  • Bleaching or topical fluoride treatment within last six months
  • Severely rotated study teeth limiting facial surface appearance
  • Visible signs of caries, fluorosis, hypocalcification, or other developmental defects
  • Restorations on the front surface of study teeth
  • Systemic or endocrine conditions such as cardiac pacemakers or diabetes mellitus
  • Craniofacial anomalies or clefts

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Baghdad - College of Dentistry / Orthodontic Clinic

Baghdad, Iraq

Actively Recruiting

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Research Team

H

Heba Tahseen Almasri, BSc, MSc (candidate)

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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