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| Name | Class |
|---|---|
| Coordenação de Aperfeiçoamento de Pessoal de NÃvel Superior. | OTHER_GOV |
Aim: The aim of this study was to compare the analgesic efficacy of two combinations of opioid and non-opioid analgesics for acute periradicular abscesses.
Methodology: This study included 24 patients who sought emergency care in a Brazilian dental school. The patients were randomly divided into two groups: Codeine/Acetaminophen - oral prescription of codeine (30 mg) plus acetaminophen (500 mg), every 4 h, for 3 days or Tramadol/Acetaminophen - oral prescription of tramadol hydrochloride (37.5 mg) plus acetaminophen (500 mg) on the same schedule. Patients recorded pain scores in a pain diary 6, 12, 24, 48, and 72 h after treatment, using the Visual Analogue Scale.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Co/ Ac | Active Comparator | Codeine/acetaminophen (30 mg/500 mg) analgesic association tablets. Patients in this group received one fixed-dose oral tablet of codeine/acetaminophen (30 mg/500 mg) every 4 hours for 3 days. |
|
| Tr/ Ac | Experimental | Tramadol/acetaminophen (37.5 mg/325 mg) analgesic association tablets. Patients in this group received one fixed-dose oral tablet of tramadol/acetaminophen (37.5 mg/325 mg) every 4 hours for 3 days. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fixed-dose oral tablet of codeine/ acetaminophen every 4 hours for 3 days | Drug | Patients in this group received opioid/ non-opioid analgesic combination. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Reduction of pain scores over time. | Pain scores were obtained using VAS before and after the first appointment. | 0, 6, 12, 24, 48 and 72 h after first dose administration |
| Measure | Description | Time Frame |
|---|---|---|
| Frequency of additional medication | Registered in the pain diary by the patient. | Up to 72 hours |
| Adverse reactions reported by patients | Registered in the pain diary by the patient. |
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Inclusion Criteria:
Exclusion Criteria:
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| Fixed-dose oral tablet of tramadol/ acetaminophen every 4 hours for 3 days | Drug | Patients in this group received opioid/ non-opioid analgesic combination. |
|
|
| Up to 72 hours |
| ID | Term |
|---|---|
| D010482 | Periapical Abscess |
| D000377 | Agnosia |
| ID | Term |
|---|---|
| D000038 | Abscess |
| D013492 | Suppuration |
| D007239 | Infections |
| D010485 | Periapical Periodontitis |
| D010483 | Periapical Diseases |
| D007571 | Jaw Diseases |
| D009057 | Stomatognathic Diseases |
| D010510 | Periodontal Diseases |
| D009059 | Mouth Diseases |
| D010518 | Periodontitis |
| D010468 | Perceptual Disorders |
| D019954 | Neurobehavioral Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| C526278 | acetaminophen, codeine drug combination |
| C478659 | Ultracet |
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