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Therapeutic Efficacy of Pistacia atlantica essential oil in the treatment of Recurrent Aphthous Stomatitis referred to Kowsar hospitals of Sanandaj

Therapeutic Efficacy of Pistacia atlantica essential oil in the treatment of Recurrent Aphthous Stomatitis referred to Kowsar hospitals of Sanandaj in 2022

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211206053290N1
Enrollment
100
Registered
2023-04-22
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Aphthous Stomatitis. Aphthous stomatitis

Interventions

Intervention 1: Intervention group: The intervention group will be prescribed Teriadent ointment. How use it is that, The gel will be applied topically 3 times a day (with an approximate weight of 200

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: No more than 2 days have passed since the onset of aphthous ulcers. Have not used any other treatment for their wounds before going to the clinic. Patients have completed the consent to participate in the trial. Be in the age group over 18 years. People with a clear history of plague should be reported at least twice a year.

Exclusion criteria

Exclusion criteria: People are allergic to the compounds and drugs used in the trial. Failure to follow the recommended instructions during the study Patients with systemic diseases such as diabetes, asthma, renal and hepatic insufficiency, epilepsy, blood and glandular disorders as well as pregnant women Patients taking antibiotics or anti-inflammatory drugs for other reasons.

Design outcomes

Primary

MeasureTime frame
Follow-up time to observe changes and improvement in aphthous lesions will be on days zero (during the first visit to the doctor), 1 (first examination) on days 7 and 10 (follow-up) after starting treatment, which will be done by referring patients to the clinic. The studied variables include the number of wounds, the size of the wounds, the amount of pain and burning, and the amount of erythema and exudate. This information will be recorded each time the patient is examined in a special form along with the patient's demographic information. Timepoint: Follow-up time to observe changes and improvement in aphthous lesions will be on days zero (during the first visit to the doctor), 1 (first examination) on days 7 and 10 (follow-up) after starting treatment, which will be done by referring patients to the clinic. Method of measurement: Wound size will be measured by a special Williams dental probe. Also, the number of mouth ulcers will be counted at the beginning of the day and during the study period. The scale of burning and pain consists of a line of 10 cm, which means zero, no pain and 10 maximum pain. The patient determines the points that indicate pain, then from zero to that point will be measured and a numerical scale from one to 100 mm will be recorded.Pain intensity in patients will be measured based on the Visual Analog Scale (VAS). This pain scale represents a 10 cm line printed with markers at each end on a piece of paper. It is "painless" at one end and "worst pain" or "indescribable pain" at the other. The person places a cross × on the line to indicate the severity of their pain. A doctor then measures the line with a ruler to get a pain score.For children, pain scales using face images are commonly used. A child may express pain with pictures of eight different faces with different expressions. The child chooses a face that feels more in tune with their current level of pain.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Jamal Amjadi

Sanandaj University of Medical Sciences

amjadijamal@yahoo.com+98 87 3366 4654

Outcome results

None listed

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