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Comparison of the Effectiveness of Interdental Aids in Reducing Plaque in Patient with Gingivitis

Comparison of the Effectiveness of Interdental Aids in Reducing Plaque in Patient with Gingivitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241014063362N2
Enrollment
54
Registered
2025-11-14
Start date
2025-10-23
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

gingivitis. Gingivitis and periodontal diseases

Interventions

Intervention 1: Intervention group: Using a soft toothbrush (Rejoy, Iran) and toothpaste (Pooneh, Iran) along with dental floss (Oxygen, Iran) - brushing twice a day and flossing once a day. Intervent

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patient's age is between 18-50 years Patient has generalized gingivitis No history of periodontal treatment in last 6 months No history of antibiotic consumption in the last 3 months Patient is physically healthy in terms of systemic health (patient is free of any physical-motor restrictions that limit hygienic practices) Absence of inflammatory conditions in the oral mucosa such as Aphthous Ulcers and Lichen Planus No use of drugs affecting the periodontium, such as anticonvulsants, calcium channel blockers, and immunosuppressants. No history of smoking Patient's crowding is less than 4 mm

Exclusion criteria

Exclusion criteria: Failure of the patient to attend the follow-up session Identification of a systemic disease that affects periodontal conditions during the study

Design outcomes

Primary

MeasureTime frame
Full mouth plaque index. Timepoint: At the beginning of the study (before the intervention) and 4 weeks after use. Method of measurement: Percentage of plaque-bearing surfaces on existing teeth.;Bleeding index. Timepoint: At the beginning of the study (before the intervention) and 4 weeks after use. Method of measurement: Percentage of surfaces with bleeding in existing teeth during probing.;Probing depth. Timepoint: At the beginning of the study (before the intervention) and 4 weeks after use. Method of measurement: Distance from gingival margin to sulcus depth.;Ease of use (Patient satisfaction). Timepoint: 4 weeks after use. Method of measurement: Visual analog scale ( VAS ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoghaye Eslami Nosrat Abadi

Yazd University of Medical Sciences

reslami2002@gmail.com+98 35 3526 2688

Outcome results

None listed

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