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Evaluation of efficacy of an Iranian-made toothbrush in orthodontic patients

Evaluation of clinical efficacy of an Iranian-made toothbrush in fixed orthodontic patients (Randomized clinical trial)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200618047823N1
Enrollment
40
Registered
2020-07-06
Start date
2020-07-09
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

Evaluation of Plaque index (Silness & Loe), Gingival index (Silness & Loe) and Ortho-plaque index in fixed orthodontic patients.

Interventions

Intervention 1: Intervention group: Participants use an Iranian toothbrush (Confident brand, with national standard mark, ISO 9001 certification and ISO 13485 certification) for one month, twice a day

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 35 Years

Inclusion criteria

Inclusion criteria: Patients are 13-35 years old. Patients are at the end of the first phase of treatment. Patients have a fixed orthodontic appliance for at least one month. Patients are physically and mentally healthy in order to observe oral hygiene. Patient's consent to participate in the study and use of prescribed toothbrushes

Exclusion criteria

Exclusion criteria: Systemic disease History of antibiotic use over the past two months The presence of lingual arch in the lower jaw and transpalatal arch or Nance in the upper jaw and any auxillary appliance such as headgear, intrusion arch and ...

Design outcomes

Primary

MeasureTime frame
Plaque index (Silness & Loe). Timepoint: Measurement of Plaque index at the beginning of the study (before the start of the intervention) and 30, 37 and 67 days after the start of the study. Method of measurement: Disclosing tablets.;Gingival index (Silness & Loe). Timepoint: Measurement of Gingival index at the beginning of the study (before the start of the intervention) and 30, 37 and 67 days after the start of the study. Method of measurement: Williams periodontal probe.;Ortho-plaque index. Timepoint: Measurement of Ortho-plaque index at the beginning of the study (before the start of the intervention) and 30, 37 and 67 days after the start of the study. Method of measurement: Disclosing tablets.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtefeh Saffar Shahroudi

Tehran University of Medical Sciences

Atefe.saffar@yahoo.com+98 21 4279 4000

Outcome results

None listed

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