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prophylactic effect of Stachys Lavandulifolia on the rate of catching cold

Evaluation the prophylactic effect of Boiling extract of Stachys Lavandulifolia on the rate of catching cold in high school students of Birjand in winter 2012

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204119443N1
Enrollment
140
Registered
2012-07-19
Start date
2012-03-20
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

common cold. Acute nasopharyngitis [common cold]

Interventions

Intervention 1: Using boiling extract of Stachys Lavandulifolia 4mg two times a day and each time one cup for 3m in winter for case group. Intervention 2: using common tea as placebo for control grou
Prevention
Treatment - Drugs
Using boiling extract of Stachys Lavandulifolia 4mg two times a day and each time one cup for 3m in winter for case group
using common tea as placebo for control group one cup 2 times a day for 3m in winter and at the same time that case group use Stachys Lavandulifolia

Sponsors

Complementary Medicine Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 20 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: compelete health condition; age: 12-20 years; reside in the camps Exclusion criteria: chronic disease and immunocompromisation; rejection of using our regimen; Age less than 12 or more than 20

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Common cold incidence. Timepoint: Before the study and 3m after study start. Method of measurement: Questionnaire and Physical examination.

Secondary

MeasureTime frame
Work absence. Timepoint: during 3m of study. Method of measurement: Days of work absence as a result of catching a cold.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJamal Mirzaei

Complementary medicine research center

mirzaei@dr.com+98 56 1223 1801

Outcome results

None listed

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