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Comparison of low power Nd-YAG laser, Myrtus communis extract and Triadent ointment in the treatment of patients with minor and Major aphthous ulcers referred to the Tabriz faculty of dentistry

Comparison of low power Nd-YAG laser, Myrtus communis extract and Triadent ointment in the treatment of patients with minor and Major aphthous ulcers referred to the Tabriz faculty of dentistry

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230823059238N3
Enrollment
60
Registered
2024-03-12
Start date
2023-12-31
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

minor and Major aphthous ulcers. Recurrent oral aphthae

Interventions

Intervention 1: Intervention group 1: In this study, laser (wave length, 1064 nm
power, 60 mW
pulse frequency, 1800 Hz
duration, 80 seconds per treatment
dose, 6.3 J/cm2) is used. The laser is placed at a distance of 1 cm from the surface of the lesion using the long pulse method and will be moved on the surface of the lesion in a sweeping manner. The

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 70 Years

Inclusion criteria

Inclusion criteria: patients with minor and Major aphthous ulcers Being in the first three days of minor and major aphthous ulcers Not taking minor and major anti-aphthous drugs Not having systemic diseases with injuries such as minor and major aphthous Having the necessary cooperation and satisfaction to conduct research

Exclusion criteria

Exclusion criteria: Having systemic diseases such as hormonal disorders, anemia, celiac disease, etc. smokers Use of tobacco Pregnancy and breastfeeding

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: Before the start of the intervention and 1, 3 and 7 days after the intervention. Method of measurement: The severity of pain will be evaluated through visual analogue scale (VAS).;The size of lesions. Timepoint: Before the start of the intervention and 1, 3 and 7 days after the intervention. Method of measurement: The size of the lesions will be measured by placing a transparent graduated grid on the lesion, determining the border of the lesion and replacing the transparent graduated grid on 1 mm graph paper, which is a reliable method for measuring the size of the lesions.?.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShiva Shahir

Tabriz University of Medical Sciences

shivashahir1225@gmail.com+98 41 3335 5965

Outcome results

None listed

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