The objective of the study was to evaluate the efficacy, safety and tolerability of a single peroral dose of 0.5 g and 1.0 g metamizol relative to placebo and 1.0 g acetylsalicylic acid in 2 episodes of moderate tension headache.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
417
Time-interval weighted sum of pain intensity difference (SPID) on a Visual Analogue Scale (VAS)
Time frame: before and 30 minutes, 1, 2, 3, and 4 hours after drug intake
Pain intensity difference (PID) on a VAS
Time frame: before and 30 minutes, 1, 2, 3, and 4 hours after drug intake
Maximum pain intensity difference (MAXPID) on a VAS
Time frame: before and 30 minutes, 1, 2, 3, and 4 hours after drug intake
Number of patients with at least a 50% pain reduction on a VAS
Time frame: before and 30 minutes, 1, 2, 3, and 4 hours after drug intake
Time to 50% pain intensity reduction on a VAS
Time frame: before and 30 minutes, 1, 2, 3, and 4 hours after drug intake
Maximum pain relief (MAXPAR) on a Verbal Rating Scale (VRS)
Time frame: 30 minutes, 1, 2, 3, and 4 hours after drug intake
Total pain relief (TOTPAR) on a VRS
Time frame: 30 minutes, 1, 2, 3, and 4 hours after drug intake
Number of patients using rescue medication
Time frame: 2, 3, and 4 hours after drug intake
Global efficacy assessment on a VRS by the patient and investigator
Time frame: 4 hours after drug intake
Number of patients with adverse events
Time frame: up to 2 months
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