Skip to content

Saliva Changes with Mouthwashes in Braces Patients

A Comparative Evaluation of the Effects of Three Different Mouthwashes on Salivary pH of the Oral Cavity in Fixed Orthodontic Patients A Randomized Clinical Trial - Cute-PH trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103317
Enrollment
120
Registered
2026-02-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

None listed

Interventions

Intervention1: Group A Hetafu mouthwash : Group A Participants were instructed to rinse with 10 15 ml of Hetafu mouthwash twice daily for 30 seconds for 1 weeks. Control Intervention1: Group B Chlor

Sponsors

Lasarkaali pvt ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 12 30 years undergoing fixed orthodontic treatment. Patients with full-mouth fixed orthodontic appliances in both arches. Patients who have been undergoing fixed appliance therapy for a minimum of 3 months. Patients with good general health and no known systemic diseases affecting salivary secretion or pH. Patients with normal salivary flow rate. Patients with good oral hygiene and no active oral infections at the time of sample collection. Patients willing to use the allocated mouthwash according to the study protocol. Patients who provide written informed consent (and parental consent for minors).

Exclusion criteria

Exclusion criteria: Patients with systemic diseases (e.g., diabetes, Sj gren s syndrome) or conditions affecting salivary flow or composition. Patients taking medications that alter salivary flow or pH (e.g., antidepressants, antihistamines). Patients with active dental caries, periodontal disease, or oral lesions. Patients using any mouthwash, probiotic, or fluoride rinse other than the study mouthwash during the study period. Patients with removable orthodontic appliances or aligners. Patients who have undergone professional oral prophylaxis within the previous 2 weeks. Patients with a history of allergy or sensitivity to any ingredient in the study mouthwashes. Patients who are uncooperative or unwilling to comply with study instructions.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure was the difference in salivary pH levels measured at baseline and after the intervention period among the three mouthwash groups.Timepoint: T0: Baseline T1: Immediately after first use (after 5 minutes) T2: After 1 week

Secondary

MeasureTime frame
The secondary outcome was the comparison of salivary pH changes among the three mouthwash groups over time.Timepoint: T0: Baseline T1: Immediately after first use (after 5 minutes) T2: After 1 week

Countries

India

Contacts

Public ContactDr Sruthi J

Adhiparasakthi Dental College and Hospital

sruthijeevagan@gmail.com9360756125

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026