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Completed
NCT07865416
Clinical Outcomes of Different Mouth Rinses During Clear Aligner Orthodontic Therapy
Conditions: Plaque-Induced Gingivitis, Orthodontic Treatment
Sex: All
Ages: 18 Years – 35 Years
Healthy volunteers: No
Phase: NA
Enrollment: 30
Sponsor: Manav Rachna International Institute of Research and Studies
Location: Faculty of Dental Sciences Faridabad Haryana
Summary
This pilot randomized controlled clinical trial will evaluate the feasibility and preliminary clinical effects of three mouth rinses-alum, Triphala-based herbal mouth rinse, and 0.2% chlorhexidine-in adults undergoing clear aligner orthodontic treatment.
Clear aligners and bonded attachments may contribute to plaque accumulation and gingival inflammation. Mouth rinses may provide an additional measure for controlling plaque and gingival inflammation during orthodontic treatment. Chlorhexidine is a commonly used antimicrobial mouth rinse, while alum and Triphala are being evaluated as alternative agents.
A total of 30 adults aged 18-35 years undergoing active clear aligner therapy and presenting with mild to moderate plaque-induced gingivitis will be randomly assigned in equal numbers to one of three groups. Participants will use their assigned mouth rinse twice daily for 30 days.
Gingival inflammation will be assessed using the Gingival Index, and plaque accumulation will be assessed using the Plaque Index at baseline, 15 days, and 30 days. Salivary Streptococcus mutans levels will also be assessed. Compliance with mouth-rinse use and other feasibility measures, including recruitment and retention, will be recorded.
The study is intended as a pilot trial to assess feasibility, estimate variability and preliminary treatment effects, and provide information for the design of a future adequately powered clinical trial.
Eligibility Criteria
Inclusion Criteria:
* Adults aged 18-35 years.
* Currently undergoing active clear aligner orthodontic treatment.
* Clear aligner use for at least 4 weeks before enrolment.
* Wearing clear aligners for approximately 20-22 hours per day.
* Presence of mild to moderate plaque-induced gingivitis, defined as a Löe and Silness Gingival Index score of 1-2.
* Presence of at least 20 natural teeth.
* Willingness to comply with the study protocol and study instructions.
* Ability and willingness to provide written informed consent.
Exclusion Criteria:
* Use of systemic antibiotics within the previous 3 months.
* Use of antimicrobial mouth rinses within the previous 1 month.
* History of periodontal pockets greater than 3 mm.
* Systemic diseases that may affect periodontal health.
* Current smoking or tobacco use.
* Pregnancy or lactation.
* Known allergy or hypersensitivity to any component of the study mouth rinses.
* Current use of systemic medications that may affect salivary flow or gingival status.
Source: ClinicalTrials.gov (NCT07865416). StuddyBuddy aggregates publicly available trial information.