The effect of herbal inhalation of Hydroalcoholic Extract of lavender, Coriandrum sativum, Zataria multiflora, Mentha piperita, in treatment of Sinus Headache

Clinical assessment of herbal inhalation of Hydroalcoholic Extract of lavender, Coriandrum sativum, Zataria multiflora, Mentha piperita, in treatment of Sinus Headache: A Randomized Double Blind Clinical Trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20170705034918N2

Enrollment

Registered

2018-09-09

Start date

2018-02-20

Completion date

Unknown

Last updated

2018-10-11

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

Conditions

Sinus Headache. Chronic sinusitis

Interventions

Intervention 1: In the intervention group, every 8 hours, patients add 5 ml of the drug to 250 ml of boiling water and inhale the vapor of it for 15 minutes and the patients and researchers will not b

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: People with a history of sinusitis assessed by the physician. People with no history of migraine headaches. People having at least three other symptoms of sinusitis such as nasal congestion. People with pain in one or more than one sinuses.

Exclusion criteria

Exclusion criteria: People who have ulcer in their mouth and nose. People Having a history of allergy

Design outcomes

Primary

Measure	Time frame
Headaches. Timepoint: Before and two weeks after the intervention. Method of measurement: Based on VAS criteria.;Rhinorrhea. Timepoint: Before and two weeks after the intervention. Method of measurement: Self-reported.;Nasal congestion. Timepoint: Before and two weeks after the intervention. Method of measurement: Self-reported.;Dyspnea. Timepoint: Before and two weeks after the intervention. Method of measurement: Self-reported.	—

Measure

Time frame

Headaches. Timepoint: Before and two weeks after the intervention. Method of measurement: Based on VAS criteria.;Rhinorrhea. Timepoint: Before and two weeks after the intervention. Method of measurement: Self-reported.;Nasal congestion. Timepoint: Before and two weeks after the intervention. Method of measurement: Self-reported.;Dyspnea. Timepoint: Before and two weeks after the intervention. Method of measurement: Self-reported.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Heidari-soureshjani

Shahre-kord University of Medical Sciences

heidari.reza1995@gmail.com+98 38 3333 6539

Outcome results

None listed

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