Efficacy of Euminz® for Tension-Type Headache - Full Text View

Purpose

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

Condition	Intervention	Phase
Episodic Tension-Type Headache	Drug: Euminz® Drug: Placebo	Phase 4


Study Type:	Interventional
Study Design:	Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Participant, Care Provider, Investigator) Primary Purpose: Treatment
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

Resource links provided by NLM:

MedlinePlus related topics: Headache

Drug Information available for: Peppermint oil

U.S. FDA Resources

Further study details as provided by Rainer Stange, Charite University, Berlin, Germany:

Primary Outcome Measures:

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). [ Time Frame: 2 hours ]
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).

Secondary Outcome Measures:

Further headache attacks will be documented and evaluated during study duration (VPRS, VAS) and described as sum of pain intensity differences (SPID) [ Time Frame: 10 weeks ]

Other Outcome Measures:

Safety [ Time Frame: 48 hours ]
Physical eximanations, overall assessments both by the patients and the investigator, vital signs, adverse events.


Enrollment:	211
Study Start Date:	February 2013
Study Completion Date:	September 2015
Primary Completion Date:	September 2015 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
Active Comparator: Euminz® Acute treatment (3 to 5 time topical use of Euminz® = 10%ethanolic solution of peppermint oil) will start immediately after assessment of a baseline pain intensity of at least moderate pain (3 on VPRS).	Drug: Euminz® 3 to 5 time topical use of study drug. Other Name: Peppermint oil (10% ethanolic solution).
Placebo Comparator: Placebo Acute treatment (3 to 5 time topical use of Placebo= 0,5% ethanolic solution of peppermint oil) will start immediately after assessment of a baseline pain intensity of at least moderate pain (3 on VPRS).	Drug: Placebo 3 to 5 time topical use of study drug. Other Name: Peppermint oil (0,5% ethanolic solution).

Detailed Description:

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).

Eligibility


Ages Eligible for Study:	18 Years to 65 Years (Adult)
Sexes Eligible for Study:	All
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Male and female patients from 18 years onwards
History of ETTH for at least one year. The number of days with such a headache is ≥2 per month
Onset of TTH below 65 years of age
At least 10 previous headache attacks fulfilling the following four inclusion criteria:
Patients with headache attacks lasting from 30 minutes to 7 days
At least two of the following pain characteristics are present:
- Pressing or tightening (non-pulsating) quality
- Intensity of pain: moderate = unable to ignore (pain may inhibit, but does not prohibit activities)
- Bilateral location
- No aggravation by walking stairs or similar routine physical activity
Headache is not accompanied by nausea or vomiting (anorexia may occur)
Headache is not accompanied by a combination of the following symptoms: photophobia and phonophobia (only one may be present)
3 months retrospective history
Willingness and ability to keep the patient's diary and to comply with the procedures of the study
Written informed consent

Exclusion Criteria:

Headaches other than TTH: (e.g. migraine, cluster headache, hypertension headache, drug-related headache,analgesic-induced headache,post-traumatic headache; associated migraine attacks are permitted if they are well recognized by the patient and if their frequency during the preceding year has not exceeded one per month)
Presence of oromandibular dysfunction
History of facial or cranial surgery
Use of prophylactic drugs for headache within one month prior to enrolment
Use of drugs for acute TTH treatment for ≥ 10 days of headache per month
Anticipated problems in adhering to the self-observation procedure (e.g. because of work)
Abuse of alcohol, narcotics or other drugs
Serious illnesses within the last 3 months (e.g. myocardial infarction, cardiac insufficiency NYHA III and IV, low blood pressure, cerebral insult, diabetes mellitus, neuropathy, changes in the skin or neoplasms in the head)
Epilepsy
Intake of anti-psychotic, anti-depressant or anti-epileptic medication during the previous month
Intake of long-acting non-steroidal anti-inflammatory drugs within the last month
Planned start of new pharmacological or non-pharmacological therapies
Any significant skin condition affecting face or neck
Known hypersensitivity towards peppermint oil
Previous use of Euminz® or any other essential oil solutions for headache in the last three months
Participation in another clinical trial within the last month
Accommodation in an institution at judicial or official request

Contacts and Locations

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01770080

Locations


Germany
Charité, Chair of Complementary and Integrative Medicine
Berlin, Germany, 14109

Sponsors and Collaborators

Charite University, Berlin, Germany

Cassella-med GmbH & Co. KG

Investigators


Study Director:	Yatin Shah, MD	Charite University, Berlin, Germany

More Information


Responsible Party:	Rainer Stange, Dr. med., Charite University, Berlin, Germany
ClinicalTrials.gov Identifier:	NCT01770080 History of Changes
Other Study ID Numbers:	2011-004777-89
Study First Received:	January 9, 2013
Last Updated:	December 29, 2015

Additional relevant MeSH terms:


Headache Tension-Type Headache Pain Neurologic Manifestations Nervous System Diseases Signs and Symptoms Headache Disorders, Primary Headache Disorders Brain Diseases	Central Nervous System Diseases Pharmaceutical Solutions Peppermint oil Antiemetics Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Gastrointestinal Agents Parasympatholytics

ClinicalTrials.gov processed this record on June 28, 2017

Efficacy of Euminz® for Tension-Type Headache (CAS/B/016611)