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The purpose of this study is to evaluate the efficacy and safety of BALI association in the treatment of aphthous ulceration.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| BALI 25 + 25 + 15 | Experimental | Three applications per day or more in case of pain, not exceeding six applications per day. The number of drops varies according to the ulcer diameter: 1 to 3 mm: 1 drop; 3 to 6 mm: 2 drops; greater than 6 mm: 3 drops. |
|
| PLACEBO | Placebo Comparator | Three applications per day or more in case of pain, not exceeding six applications per day. The number of drops varies according to the ulcer diameter: 1 to 3 mm: 1 drop; 3 to 6 mm: 2 drops; greater than 6 mm: 3 drops. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BALI association | Drug | BALI association oral suspension, 25 mg + 25 mg + 15 mg, oral. Three applications per day or more in case of pain, not exceeding six applications per day. |
|
| Measure | Description | Time Frame |
|---|---|---|
| To assess the reduction in pain intensity after 3 days of treatment. | Difference in pain intensity after 3 days of treatment compared to baseline. Pain intensity will be evaluated by the Visual Analogue Scale (VAS). The VAS consists of a 10 cm line, with two end points representing 0 ("no pain") and 10 (pain as bad as it could possibly be"). | 3 days |
| Measure | Description | Time Frame |
|---|---|---|
| To assess the reduction in pain intensity after the first application. | Difference in pain intensity 15 minutes after the first application of the medication compared to baseline, measured by the VAS scale. The VAS consists of a 10 cm line, with two end points representing 0 ("no pain") and 10 (pain as bad as it could possibly be"). | 15 minutes |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| EMS | Hortolândia | São Paulo | Brazil |
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| ID | Term |
|---|---|
| D013281 | Stomatitis, Aphthous |
| ID | Term |
|---|---|
| D013280 | Stomatitis |
| D009059 | Mouth Diseases |
| D009057 | Stomatognathic Diseases |
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| Placebo | Drug | Placebo. Three applications per day or more in case of pain, not exceeding six applications per day. |
|
| To assess the reduction in pain intensity during the treatment. | Difference in pain intensity after 5 and 7 days of treatment compared to baseline, measured by the VAS scale. The VAS consists of a 10 cm line, with two end points representing 0 ("no pain") and 10 (pain as bad as it could possibly be"). | 5 and 7 days |
| Percentage of participants healed during treatment. | Percentage of participants healed after 3, 5, and 7 days of treatment, defined as ulcer diameter = 0 mm and pain intensity = 0, measured by the Likert scale. Likert scale is a five point scale: 0 = no pain and 4 = pain as bad as it could possibly be". | 3, 5 and 7 days |
| Percentage of participants with no pain during treatment. | Percentage of participants with no pain after 3, 5, and 7 days of treatment, measured by the Likert scale. Likert scale is a five point scale: 0 = "no pain" and 4 = "pain as bad as it could possibly be". | 3, 5 and 7 days |
| To assess the percentage change in pain intensity from baseline during treatment. | Pain intensity will be evaluated by the VAS scale.The following calculations will be performed: ((D3, D5 or D7 - V0) / baseline) ×100%. The VAS consists of a 10 cm line, with two end points representing 0 ("no pain") and 10 (pain as bad as it could possibly be"). | 3, 5 and 7 days |