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The effect of photodynamic therapy on the Treatment of ulcerative-erosive oral lichen planus

The effect of adding photodynamic therapy to corticosteroid mouthwash on the Treatment of ulcerative-erosive oral lichen planus

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150609022628N1
Enrollment
36
Registered
2025-07-19
Start date
2025-05-13
Completion date
Unknown
Last updated
2025-08-19

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: Control Group : The Control group Patients receive mouthwash containing corticosteroid (0.5 mg of dexamethasone in 5 ml of water) as a standard first-line treatment
Then 30 minutes later, 100,000 units of nystatin solution is applied to prevent candidiasis. Treatment with mouthwash is done 4 times a day. In addition, patients are treated with sham photodynamic th
Then, after 15 minutes, the lesion and 0.5 mm around the lesion a re exposed to sham laser (placebo) In a way that the patient is unaware laser unit is off due to wearing protective eyewear. In order
Then, 30 minutes later, 100,000 units of nystatin solution is applied to prevent candidiasis. Treatment with mouthwash is done 4 times a day. In addition, patients in the intervention group are treate

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with ulcerative-erosive oral lichen planus, whose disease was confirmed by histopathological examination.

Exclusion criteria

Exclusion criteria: Lesions that have evidence of dysplasia in the histopathological view contact or medicinal lichenoid lesions patients who have received oral treatment for their lichen planus during the last month pregnant and lactating patients people with uncontrolled systemic disease photosensitive people

Design outcomes

Primary

MeasureTime frame
Pain Score. Timepoint: Before starting intervention , one week, two weeks, one month and two months after starting intervention. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Lesion size score. Timepoint: Before starting intervention, one week, two weeks, one month and two months after starting intervention. Method of measurement: Graded abslang.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFaezeh Khozeimeh

Esfahan University of Medical Sciences

khozeimeh@dnt.mui.ac.ir+98 31 3792 5514

Outcome results

None listed

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