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Treating Patients with Dental Caries using Herbal Mouthwash Oxirinse in Comparison with Listerine Mouthwash

â??A Prospective Randomized, Parallel Design, Controlled Study To Evaluate The Efficacy And Safety of Herbal Mouthwash Oxirinse Dispersible Tablet in Comparison with Listerine Mouthwash in Treating Patients with Dental Cariesâ??

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/11/016358
Enrollment
34
Registered
2018-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K029- Dental caries, unspecified

Interventions

Intervention1: Oxirinse Dispersible tablet: Dose: 20 ml, Route of administration: Oral, Frequency: Once a day Total duration of therapy: 1 Day Control Intervention1: Listerine Mouthwash: Dose: 20 ml,

Sponsors

Avance Phytotherapies Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Willing to participate by providing written informed consent 2. Patients with high caries risk 3. Good general health with (in the opinion of the investigator) no clinically significant and relevant abnormalities of medical history or oral/ dental examination. 4. Patient having at least 12 gradable teeth. 5. Patient in agreement to delay any elective dental treatment including oral prophylaxis 6. Is the patient having ability to understand and consent to participate in this clinical study, expressed by signing the consent form? 7. Patient ready to comply with the study visits were included in the study

Exclusion criteria

Exclusion criteria: 1. History of systemic diseases 2. History of oral prophylaxis within 6 months previous to the study 3. Known or suspected intolerance or hypersensitivity to Chlorhexidine or other study materials (or closely related compounds) or any of their stated ingredients. 4. Patient with mouth breathing habit 5. Patient using orthodontic and prosthodontic appliances

Design outcomes

Primary

MeasureTime frame
Salivary pH Salivary buffer capacity Microbial count of saliva Timepoint: Visit1 day1 visit2 day3

Secondary

MeasureTime frame
Dysgeusia Transient burning/stinging of mucous membrane secondary to mouth rinse Timepoint: Visit1 day1 visit2 day3

Countries

India

Contacts

Public ContactDr Suvodip Shaw

iDD Research Solution INC

yogesh@iddresearch.com

Outcome results

None listed

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