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Therapeutic effects of Stinging Nettle (Urtica dioica)

Not Applicable
Conditions
Hyperandrogenism.
Hypersecretion of Ovarian Androgens
Registration Number
IRCT2013061013612N1
Lead Sponsor
Bone Research Center, Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
40
Inclusion Criteria

women with hyperandrogenism ; ages between 15-50 Exclusion criteria: The period of lactation ; pregnancy

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum level of free Testestrone. Timepoint: Before study and after 4 months. Method of measurement: Lab test , ng/dl.;Serum level of total Testestrone. Timepoint: Before study and after 4 months. Method of measurement: Lab test , ng/dl.;Serum level of DHEA. Timepoint: Before study and after 4 months. Method of measurement: Lab test , ng/dl.
Secondary Outcome Measures
NameTimeMethod
Edema. Timepoint: Every month. Method of measurement: History and Examination.;Gastrointestinal Complaints. Timepoint: Every month. Method of measurement: History and Examination.;Decreased urine volume. Timepoint: Every month. Method of measurement: History and Examination.
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