Efficacy and Safety Study to Compare Ibuprofen + Caffeine With Ibuprofen Alone in the Treatment of Headache
A Clinical Multicenter, Phase III, Randomized, Double-blind, Prospective and Comparative Trial to Evaluate the Efficacy and Safety of the Combination of Ibuprofen + Caffeine in the Treatment of Headache Attacks, Compared to Ibuprofen Alone.
1 other identifier
interventional
144
0 countries
N/A
Brief Summary
Based on established therapeutic effect of ibuprofen in the treatment of headache attacks, and the action of caffeine in promoting better results when combined with treatments of first choice in the treatment of headache, this study is designed to:
- evaluate the efficacy of therapy with ibuprofen + caffeine in headache patients compared to ibuprofen alone;
- evaluate the tolerability of the association ibuprofen + caffeine compared to ibuprofen alone. The hypothesis is that the association is superior to treatment with ibuprofen alone in terms of efficacy, while maintaining good tolerability.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_3
Started Oct 2010
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 28, 2010
CompletedFirst Posted
Study publicly available on registry
July 29, 2010
CompletedStudy Start
First participant enrolled
October 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2012
CompletedJuly 29, 2010
July 1, 2010
2 years
July 28, 2010
July 28, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Efficacy of study treatment compared with control to relieve headache symptoms.
The evaluation of efficacy will be determined based on comparison of the intensity of headache before and after initiation of treatment, using the Functional Disabling Scale. The opinion of the investigator will be established based on the Likert scale and duration of symptoms after the treatment will be checked as a measure of comparison between treatments in the study.
4 weeks
Secondary Outcomes (1)
Tolerability of study treatment compared with control to relieve headache symptoms.
4 weeks
Study Arms (2)
Ibuprofen + Caffeine
EXPERIMENTAL72 patients treated with one or two tablets of ibuprofen 400 mg + caffeine 200 mg when presenting headache.
Ibuprofen
ACTIVE COMPARATOR72 patients treated with one or two tablets of ibuprofen 400 mg when presenting headache.
Interventions
One or two tablets of ibuprofen 400 mg + caffeine 200 mg when presenting headache.
One or two tablets of ibuprofen 400 mg when presenting headache.
Eligibility Criteria
You may qualify if:
- Patients with ability to read, understand and sign the IC;
- Patients with symptoms of frequent episodic tension headache, mild to moderate;
- Patients with symptoms of migraine with or without aura, of mild to moderate intensity;
- Patients who have had between two and five headache attacks in the last 30 days;
- Patients who accept the condition of ingesting less than three cups of coffee per day and / or reduce the intake of any beverage that contains caffeine;
- Patients who accept the condition not to drink any beverage that contains caffeine for 24 hours after drug administration.
- Patients able to understand and maintain the clinical protocol.
- Female patients of childbearing age must agree to undergo pregnancy testing through urine.
You may not qualify if:
- Patients in whom headache began after 50 years of age;
- Patients with strong or disabling headaches;
- Patients with chronic daily headaches lasting up to 72 h or with cluster headaches not responsive to common analgesics;
- Patients with headaches occurring in 15 or more days per month;
- Patients with secondary headaches;
- Patients who overuse analgesics (acetylsalicylic acid up to 300 mg / day) or NSAIDs;
- Known hypersensitivity to components of both formulations of the drug test as the comparison;
- Known hepatic or renal diseases;
- Patients who are pregnant or intend to become pregnant or lactating;
- Patients with severe concomitant systemic diseases such as cancer, diabetes, congenital or acquired heart diseases, hematological diseases, convulsive disorders, autoimmune diseases, renal failure, severe infections, hormonal disorders, pulmonary disorders and peptic diseases;
- History of alcoholism or substance abuse.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
July 28, 2010
First Posted
July 29, 2010
Study Start
October 1, 2010
Primary Completion
October 1, 2012
Study Completion
October 1, 2012
Last Updated
July 29, 2010
Record last verified: 2010-07