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Effect of Iranian Traditional Medicine drugs in the treatment of Migraine.

Efficacy of “Etrifel” and “Mastaki” on monthly bouts of headache in Migraineurs with Gastric Headache.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015092324150N1
Enrollment
30
Registered
2017-01-08
Start date
2017-01-04
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Migraine. Migraine

Interventions

Etrifel confection, 10 grams(or maximum tolerated dose), once daily for 12 weeks, orally, before breakfast. Mastic gum powder, 3 grams(or maximum tolerated dose), once daily for 12 weeks, orally, befo
Treatment - Drugs

Sponsors

Deputy of Research and Technology of Shahed university
Lead Sponsor
Barij Essence Pharmaceutical Company (R&D division)
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Male or female 18-65 years old; diagnosed since 6 months ago with Episodic or Probable Migraine ± aura by a specialist according to criteria from ICHD-III; having 3 to 14 attacks of migraine in a month from 3 months ago; diagnosed with Gastric Headache according to Iranian Traditional Medicine Questionnaire; normal neurologic examination Exclusion criteria: Taking preventive drugs in the last 3 months; history of drug abuse; history of allergy to the trial drugs; pregnant or breast feeding women; systemic and other neurologic diseases

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache frequency in a period of 4 weeks. Timepoint: before intervention, 4, 8, and 12 weeks after the start of intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Headache severity. Timepoint: before intervention, 4, 8, and 12 weeks after the start of intervention. Method of measurement: Visual Analgue Scale.;Headache duration. Timepoint: before intervention, 4, 8, and 12 weeks after the start of intervention. Method of measurement: Questionnaire.;The amount of rescue medication use in each attack. Timepoint: before intervention, 4, 8, and 12 weeks after the start of intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Talafi Noghani

Iranian Traditional Medicine Department, Shahed university

M.Noghani@Shahed.ac.ir+98 21 5121 4055

Outcome results

None listed

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