Skip to content

Effect of Valerian on tension headache

A review of tension headaches in Iranian medicine and comparison the effects of the of Valerian extraction and placebo on severity and duration of headaches in patients with tension-type headache

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171203037738N1
Enrollment
110
Registered
2018-03-16
Start date
2018-04-21
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tension Headache. Chronic tension-type headache

Interventions

Intervention 1: Intervention group: Valeriana capsule contain 530 mg Valeriana root powder. Intervention 2: Control group: placebo capsule contain 50 mg breadcrumbs powder.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Complete written informed consent Age between 18 to 65 years Suffering from common or chronic tension headache based on the International Association Headache (ICHD-III) criteria Be under treatment with medications Not completed treatment (for headache) Informed consent

Exclusion criteria

Exclusion criteria: Patients with uncommon or probable headache or other primary or secondary headaches Headache increases with head movement Metabolic or musculoskeletal disorders that cause similar headache symptoms History of trauma to the spinal cord True or false vertigo Rigidity of the joints, atherosclerosis or advanced arthritis Emotional stress Neurological disorders Taking barbiturates or sedative medications (classic or traditional medicine) The consumption of valerian or its products in the past month Pregnancy and lactation Having underlying disease including diabetes, hypertension, heart disease, liver and kidney disease, and chronic psychological disease History of hypotension (with or without medication) Use of anticoagulants, antiplatelet, heparin, thrombotic agents, opioid analgesics and loperamide Patient headaches improve with taking triptans

Design outcomes

Primary

MeasureTime frame
Frequency of headache and disability caused by headache are our main outcomes measures. Timepoint: Per 4 weeks. Method of measurement: We will employ HDI and HIT-6 questionnaires.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHosain Azizi

Iran University of Medical Sciences

azizitarin@gmail.com+98 51 5224 5762

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026