Episodic Tension-Type Headache Clinical Trial
Official title:
Efficacy and Safety of Euminz® (10% Ethanolic Solution of Peppermint Oil for Topical Use) Compared to Placebo in Patients With Episodic Tension-type Headache (ETTH); Phase IV Clinical Trial
Efficacy and safety of Euminz® (10% ethanolic solution of peppermint oil for topical use)
compared to placebo in patients with episodic tension-type headache (ETTH).
Prospective, double-blind, placebo-controlled, phase IV clinical trial; Parallel-groups
design; Randomisation 1:1; First attack per patient will be evaluated for primary
objectives, following attacks during study duration will be observed and documented.
Study duration per patient: 10 weeks
To demonstrate the efficacy of Euminz® to reduce the intensity of headache symptoms
experienced by patients with episodic tension-type headache. The two primary objectives will
be tested hierarchically (a-priory ordered) to avoid alpha-adjustment:
First primary objective of the first headache episode is "pain-free" (0 or 1) after 2 hours
measured on a six-step verbal pain rating scale (VPRS). Acute treatment (3 to 5 time topical
use of Euminz®) will start immediately after assessment of a baseline pain intensity of at
least moderate pain (3 on VPRS).
Second primary objective of the first headache episode will be the decrease of intensity of
pain measured by a visual analogue scale (VAS). The difference from measure point 0 (before
first application of Euminz®) on the VAS in comparison to 15, 30, 45, 60, 90 and 120 minutes
after start of treatment will be shown as area under the curve representing the pain
intensity difference (PID).
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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