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Effect of Ferula Assafoetida on polycystic ovarian syndrome

Effect of Ferula assafoetida on clinical and paraclinical indices of polycystic ovarian syndrome and its comparison with LD tablet.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190728044360N1
Enrollment
30
Registered
2019-12-11
Start date
2019-12-11
Completion date
Unknown
Last updated
2019-12-17

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

Conditions

Polycystic ovarian syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: Case group: This group will be treated with Ferual Assafoetida (1 gram daily) for three weeks and discontinue the consumption for one week. Thereafter, patients will use the drugs for

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 40 Years

Inclusion criteria

Inclusion criteria: All 15 to 40 years old women with polycystic ovarian syndrome

Exclusion criteria

Exclusion criteria: Pregnancy Allergy to Ferula Asafoetida Diabetic patients Thyroid diseases

Design outcomes

Primary

MeasureTime frame
Presence of ovarian cysts. Timepoint: Before Intervention and seven days after Intervention. Method of measurement: Sonography.;Occurrence of menstrual bleeding. Timepoint: 4 and 8 weeks after the beginning of treatment. Method of measurement: asking.;Hirsutism. Timepoint: Before Intervention and seven days after Intervention. Method of measurement: Ferriman–Gallwey scale.

Secondary

MeasureTime frame
Body mass index. Timepoint: Before Intervention and seven days after Intervention. Method of measurement: Meter and scale.;Total Testosterone. Timepoint: Before Intervention and seven days after Intervention. Method of measurement: CLIA laboratory method.;Free Testosterone. Timepoint: Before Intervention and seven days after Intervention. Method of measurement: ELIZA laboratory method.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNajmeh Dehparvar

Shahed University

n.dehparvar@shahed.ac.ir+98 25 3770 1938

Outcome results

None listed

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