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Investigation effect of Silybum marianum and Panax ginseng on allergic rhinitis.

Investigation effect of Silybum marianum and Panax ginseng on clinical signs and symptoms of allergic rhinitis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201511206252N10
Enrollment
180
Registered
2015-12-17
Start date
2015-07-23
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

Allergic rhinitis. Allergic rhinitis, unspecified

Interventions

Intervention 1: The intervention group 2 are prescribed Silybum marianum capsule 140mg two times daily and standard medication. Intervention 2: The control group are prescribed standard medication onl
Treatment - Drugs
The intervention group 2 are prescribed Silybum marianum capsule 140mg two times daily and standard medication.
The control group are prescribed standard medication only.
The intervention group 1 are prescribed Panax ginseng capsule 500mg two times daily and standard medication.

Sponsors

Vice Chansellor for Research, Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18-55 year old paitients with allergic rhinitis for two last years. Exclusion criteria: Paitients with cardiac diseasis, asthma, high blood pressure, diabet melitus. Pregnancy and lactation. Paitients who use asprin, varfarin, anti hypertensive drugs and anti phsycotic drugs.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sneezing. Timepoint: first day,seventh day,forteenth day,thirtieth day. Method of measurement: clinical evaluation.;Nasal discharge. Timepoint: first day,seventh day,forteenth day,thirtieth day. Method of measurement: clinical evaluation.;Nasal itching. Timepoint: first day,seventh day,forteenth day,thirtieth day. Method of measurement: clinical evaluation.

Secondary

MeasureTime frame
Nasal obstraction or congestion. Timepoint: first day,seventh day, fourteenth day, thirtieth day. Method of measurement: clinical evaluation.;Occular itching. Timepoint: first day,seventh day, fourteenth day, thirtieth day. Method of measurement: clinical evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoroush Amani MD

Shahrekord University of Medical Sciences

info@Skums.ac.ir+98 38 3333 0061

Outcome results

None listed

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