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Evaluation of the effect of adding low level laser irradiation to drug therapy in patients affected with burning mouth syndrome: A randomized clinical trial

Evaluation of the effect of adding low level laser irradiation to drug therapy in patients affected with burning mouth syndrome: A randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200905048623N1
Enrollment
46
Registered
2020-09-21
Start date
2019-10-23
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

Burning mouth syndrome. Other and unspecified lesions of oral mucosa

Interventions

Intervention 1: Intervention group 1: The drug given to all patients is citalopram, the initial dose of which is 10 mg and after one week it is increased to 20 mg and used once a day for one month an

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients are diagnosed with burning mouth syndrome. Patients are systemically healthy. Patients with normal oral mucosa should be examined clinically. Patients have a burning sensation daily 4 to 6 months with constant or increased intensity during the day.

Exclusion criteria

Exclusion criteria: Patients with systemic problems manifested by burning mouth, such as diabetes, severe anemia, vitamin deficiency. There are contraindications to laser administration such as pregnancy, epilepsy, cancer, chemotherapy. Patients with severe psychiatric disorders, such as major depression

Design outcomes

Primary

MeasureTime frame
The amount of mouth burning is measured by asking the patient using a 0 to 10 graduated ruler. Timepoint: The severity of burning will be measured before the start of treatment and at the end of each week after treatment (first week, second week, third week, fourth week) and the end of the third month. Method of measurement: Patient questions are measured using the Visual Analogue Scale, a scale from 0 to 10.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHooman Ebrahimi

Islamic Azad University

Hooman.ebrahimi@yahoo.com+98 21 8804 3288

Outcome results

None listed

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