Efficacy and Safety of a Fixed-dose Combination of Naratriptan and Naproxen in Acute Treatment of Migraine
Overview[ - collapse ][ - ]
| Purpose | The purpose of this study is to determine whether a fixed-dose combination of naratriptan + naproxen is effective compared each monotherapy for the acute treatment of migraine. |
|---|---|
| Condition | Migraine Headache |
| Intervention | Drug: Fixed-dose combination of naratriptan + naproxen Drug: Naratriptan Drug: Naproxen |
| Phase | Phase 3 |
| Sponsor | Ache Laboratorios Farmaceuticos S.A. |
| Responsible Party | Ache Laboratorios Farmaceuticos S.A. |
| ClinicalTrials.gov Identifier | NCT01390324 |
| First Received | July 7, 2011 |
| Last Updated | August 18, 2011 |
| Last verified | July 2011 |
Tracking Information[ + expand ][ + ]
| First Received Date | July 7, 2011 |
|---|---|
| Last Updated Date | August 18, 2011 |
| Start Date | December 2011 |
| Estimated Primary Completion Date | Not Provided |
| Current Primary Outcome Measures | Headache relief 2 hours after dosing, without use of rescue medication. [Time Frame: 2 hours after single dose of double-blind treatment] [Designated as safety issue: No]Participants were evaluated (self-assessment) for pain intensity by using a 4-point rating scale: 0=none, 1=mild, 2=moderate, and 3=severe. |
| Current Secondary Outcome Measures |
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Descriptive Information[ + expand ][ + ]
| Brief Title | Efficacy and Safety of a Fixed-dose Combination of Naratriptan and Naproxen in Acute Treatment of Migraine |
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| Official Title | A Multicenter, National, Double-blind, Randomized Study to Evaluate the Efficacy and Safety of a Fixed-dose Combination of Naratriptan 2,5 mg + Naproxen 500 mg Relative to Efficacy and Safety of Each Monotherapy for the Acute Treatment of Migraine |
| Brief Summary | The purpose of this study is to determine whether a fixed-dose combination of naratriptan + naproxen is effective compared each monotherapy for the acute treatment of migraine. |
| Detailed Description | Not Provided |
| Study Type | Interventional |
| Study Phase | Phase 3 |
| Study Design | Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment |
| Condition |
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| Intervention | Drug: Fixed-dose combination of naratriptan + naproxen Tablets containing naratriptan 2,5 mg + naproxen 500 mg Drug: Naratriptan Tablets containing naratriptan 2,5 mg Drug: Naproxen Tablets containing naproxen 500 mg |
| Study Arm (s) |
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Recruitment Information[ + expand ][ + ]
| Recruitment Status | Not yet recruiting |
|---|---|
| Estimated Enrollment | 564 |
| Estimated Completion Date | Not Provided |
| Estimated Primary Completion Date | October 2012 |
| Eligibility Criteria | Inclusion Criteria: - Male or female patient, age in the range of 18-65 years inclusive that has onset of migraine before age 50; - Patient has at least a 3-month history of migraine with or without aura according to the ICHD-II, 2004, IHS (International Headache Society) criteria; - Patients experienced an average migraine headache frequency of 2-6 moderate or severe attacks per month in the last 03 months prior to screening visit; - Patients able to distinguish his/her migraine attacks from any other types of headaches; - Patients able to understand and consent to participate in this clinical study, expressed by signing the Informed Consent (IC). Exclusion Criteria: - History of more than 6 migraine attacks/month in the last 03 months prior to screening visit; - History of non-migraine headache frequency ≥ 15 days/month in each of the 3 months prior to screening. - History of following migraine variants, according to the ICHD-II, 2004, IHS (International Headache Society): basilar migraine, aura without headache, familial hemiplegic migraine, sporadic hemiplegic migraine or aura with non-migraine headache; - If female of childbearing potential, has a negative urine pregnancy test at Visit 0 and uses, or agrees to use, for the duration of the study, a medically acceptable form of contraception as determined by the investigator; - Woman in pregnancy or lactation period; - History of epilepsy or psychiatric condition that may affect the compliance of the treatment; - Patients in acupuncture treatment for the symptoms of migraine attacks; - Suffers from cardiovascular disease (ischemic heart disease, including angina pectoris, myocardial infarction, documented silent ischemia, or with Prinzmetal's angina) or has symptoms of ischemic heart disease; - History of cerebrovascular pathology including stroke and/or transient ischemic attacks; - History of allergic reactions to naproxen preparations, including subjects in whom aspirin or other NSAID drugs induce the syndrome of asthma, rhinitis, nasal polyps or urticaria; - Diagnosis of renal or hepatic failure; - Has significant (as determined by the investigator) cardiovascular risk factors that may include uncontrolled high blood pressure, post-menopausal women, males over 40 years old, hypercholesterolemia, obesity, diabetes mellitus, smoking, or a family history of cardiovascular disease in a 1st degree relative. - Patients who have stopped or changed the dosage of the preventive treatment of migraine in the last 2 weeks prior the screening visit (V0), including the use of calcium channel blockers, tricyclic antidepressants, beta blockers or serotonergic medications for any other indications; - Use of prohibited medicine as shown in 9.3 item of this protocol; - Inability to understand and report the categorical scale debilitating functional of study or symptoms diary; - Has abused, in the opinion of the Investigator, any of the following drugs, currently or within the past 2 years: opioids, alcohol, barbiturates, benzodiazepine, cocaine or abuse of drugs for migraine treatment including narcotics ergotamines headache in the past 03 months; - Hypersensitivity, intolerance, or contraindication to the use of naratriptan or naproxen, any of its components; - Hypersensitivity, intolerance, or contraindication to the use of sulfonamides; - History of malignancy ≤ 5 years or > 5 years without documentation of remission / cure, for example, melanoma, leukemia, lymphoma, myeloproliferative disorders and renal cell carcinoma of any duration. Exception: Subjects with basal cell skin cancers, squamous cell, and cervical cancer in situ may be eligible; - Participation in last one year of clinical protocols, unless it can be direct benefit to patient; - Any finding of clinical observation (anamnesis and physical exam) laboratory abnormality (eg, blood glucose, blood count), disease (for example, liver, cardiovascular system, lung) or therapy that, in opinion of the investigator, may endanger the patient or interfere with the endpoints of study. |
| Gender | Both |
| Ages | 18 Years |
| Accepts Healthy Volunteers | No |
| Contacts | Contact: Carla R Peron, Physician +55 11 2608-8680 carla.peron@ache.com.br |
| Location Countries | Not Provided |
Administrative Information[ + expand ][ + ]
| NCT Number | NCT01390324 |
|---|---|
| Other Study ID Numbers | ACH-NRP-03(05/11) |
| Has Data Monitoring Committee | No |
| Information Provided By | Ache Laboratorios Farmaceuticos S.A. |
| Study Sponsor | Ache Laboratorios Farmaceuticos S.A. |
| Collaborators | Not Provided |
| Investigators | Principal Investigator: Deusvenir S Carvalho Federal University of São Paulo |
| Verification Date | July 2011 |