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Evaluation of the effectiveness of Bamboo Salt mouthwash in the improvement of Recurrent Aphthous Ulcers

Evaluation of the Effectiveness of Bamboo Salt mouthwash compared to Non-Steroidal mouthwash in the improvement of Recurrent Aphthous Ulcers,a Double Blind Randomized Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160126026209N3
Enrollment
40
Registered
2023-04-15
Start date
2023-04-08
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

recurrent aphthous ulcers. Recurrent oral aphthae

Interventions

Intervention 1: Intervention group: Gargle 60 cc (containing 30 cc of 10% bamboo salt and 30 cc of benzydamine 0.15%) solution every 8 hours and avoid eating and drinking for at least 30 to 60 minutes

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with minor aphthous lesions less than 2 days from initiation The individuals who had not suffered from systemic diseases or immunologic disease The patient should not receive other concurrent medication for aphthous ulcers either systematically or locally at the same time with this medicine Patients who had a history of frequent recurrence of aphthous lesions The occurrence of aphthous lesions is not caused by beta blockers and NSAIDs Patients who dose not being in pregnancy or breastfeeding time Patients who have not been receiving Anti-inflammatory or immunosuppressive drugs for at least 2 weeks before the study begins Patients who have not been receiving systemic Antibiotics for at least 2 weeks before the study begins Have not treated aphthous ulcers with any other medicine in the last 3 days Patients who have not been receiving sedative medicine for other diseases

Exclusion criteria

Exclusion criteria: In case of sudden problem or violation of Inclusion criteria, the patient will be excluded from the study

Design outcomes

Primary

MeasureTime frame
Duration of lesion's pseudomembrane removing. Timepoint: The time when the pseudomembrane and the erythematous border are removed. Method of measurement: Observing the lesion.;The size of the lesion. Timepoint: The aphthous lesion size will be recorded on days 0, 1, 3, and 5. Method of measurement: Periodontal probe.;The aphthous pain level. Timepoint: The patients are asked to record the aphthous pain level on days 0, 1, 3, and 5. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Zahra Saberi

Esfahan University of Medical Sciences

zahra.saberi@dnt.mui.ac.ir+98 31 3792 5514

Outcome results

None listed

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