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Comparing the effects of cryotherapy and local corticosteroids in the treatment of oral lichen planus lesions

Comparing the effects of cryotherapy and local corticosteroids in the treatment of oral lichen planus lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012120311656N1
Enrollment
30
Registered
2012-12-23
Start date
2012-12-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Oral lichen planus.

Interventions

Intervention 1: Control Group: Topical corticosteroid in orabase. Intervention 2: Intervention: Cryotherapy with N2O gass.
Treatment - Drugs
Treatment - Devices
Control Group: Topical corticosteroid in orabase
Intervention: Cryotherapy with N2O gass

Sponsors

?Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: • Clinical diagnosis of oral lichen planus • Existence of two lesions with similar clinical appearance (with the size difference of less than 1 cm) on the right and left buccal mucosa or right and left side of tongue • Not received any treatment for the lesions for at least 2 weeks ago • Signing the consent form. Exclusion criteria: • Using drugs that are proved to develop lichenoid lesions. • Lesions seen in contact with dental amalgam • Coexisting dermal and genital lesions • Hypersensitivity to drugs being used • Pregnant women • Systemic disease such as systemic lupus erythematosus, erythema multiform, secondary syphilis, graft versus host disease or others systemic disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduction in severity of lesions. Timepoint: 2 weeks after treatment. Method of measurement: cilinical judgement of a capable cilinician.;Lesion size. Timepoint: 2, 4, 6, 8, 10, 12 weeks after treatment. Method of measurement: with a digital culis.;Pain. Timepoint: 2, 4, 6, 8, 10, 12 weeks after treatment. Method of measurement: Visual analogue score.

Secondary

MeasureTime frame
Patient satisfaction of each individual treatment. Timepoint: 3 months after treatment. Method of measurement: by asking the patient to give a percentage of satisfaction for each side.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Maryam Zahed

Shiraz University of Medical Sciences, Dental school

maryamzhd@yahoo.com+98 71 1648 6702

Outcome results

None listed

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