Preparation an oral gel-made from thymoquinone (TQ), and clinical study investigating the efficacy of it on patients with aphtha
Phase 2
Completed
- Conditions
- Recurrent Aphthous Stomatitis.Recurrent oral aphthae
- Registration Number
- IRCT2016100914106N5
- Lead Sponsor
- Vice chancellor for research, Kermanshah University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 56
Inclusion Criteria
Patient inclusion criteria include: possessing aphtatous ulcer; patients without systemic diseases, hypersensitivity history; smoking habits or alcoholism; pregnancy and lactation; orthodontic instruments.
Patient exclusion criteria include: Drug usage or any treatment occurring before dental treatment.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of healing. Timepoint: healing measurement will be done twice per month. Method of measurement: quantitative and qualitative assays.;Size of lesion. Timepoint: size of lesion measurement will be done twice per month. Method of measurement: quantitative and qualitative assays.;Pain in lesion. Timepoint: pain measurement in lesion will be done twice per month. Method of measurement: quantitative and qualitative assays.;Erythema. Timepoint: erythema evaluation will be done twice per month. Method of measurement: quantitative and qualitative assays.
- Secondary Outcome Measures
Name Time Method