Betamethasone mouthwash in the treatment of patients with oral lichen planus

Comparison of the effect of betamethasone niosomal mouthwash with non-niosomal form in treatment of oral lichen planus patients

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240804062631N1

Enrollment

Registered

2024-08-22

Start date

2024-09-10

Completion date

Unknown

Last updated

2024-08-26

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

Conditions

lichen planus. Lichen planus

Interventions

Intervention 1: Intervention group: People with lichen planus treated with Niosomal betamethasone mouthwash, three times a day for 4 hours. Intervention 2: Control group: People with lichen planus tre

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Includes ulcerative or atrophic lichen planus that is clinically or histopathologically confirmed

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Determining the average recovery period and the size of oral ulcers in oral lichen planus patients in 2 study groups. Timepoint: Determining the average healing period and the size of oral ulcers in oral lichen planus patients in 2 study groups before and after the intervention. Method of measurement: Visual analog scale.;Determining the investigated parameters in the wound in 2 studied groups. Timepoint: Determining the investigated parameters in the wound on days 1 to 8 in 2 studied groups. Method of measurement: Questionnaire.	—

Measure

Time frame

Determining the average recovery period and the size of oral ulcers in oral lichen planus patients in 2 study groups. Timepoint: Determining the average healing period and the size of oral ulcers in oral lichen planus patients in 2 study groups before and after the intervention. Method of measurement: Visual analog scale.;Determining the investigated parameters in the wound in 2 studied groups. Timepoint: Determining the investigated parameters in the wound on days 1 to 8 in 2 studied groups. Method of measurement: Questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSina Kakooei

Kerman University of Medical Sciences

kakooei.s@gmail.com+98 34 3212 6024

Outcome results

None listed

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