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Effect of Aslagh and Uriculotherapy in Polycystic Ovary Syndrom

Comparison of the Effectiveness of Aslagh Herbal Capsule (Iranian Traditional Medicine Product) and Ear Acupressure (Uriculotherapy) on the Symptoms of Polycystic Ovary Syndrome in Women aged 18-43 years

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200407046980N1
Enrollment
110
Registered
2020-04-28
Start date
2020-04-18
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Polycystic Ovary Syndrom. Polycystic ovarian syndrome

Interventions

Intervention 1: First intervention group: Consumption of Aslagh herbal capsules is proven. This capsule is a compound derived from the texts of traditional Iranian medicine, in which Daucus carata see

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 43 Years

Inclusion criteria

Inclusion criteria: Women 18-43 years old Having Rotterdam Criteria for Diagnosing Polycystic Ovary Syndrome Polycystic Ovary Syndrom Patients with Oligomenorrhea

Exclusion criteria

Exclusion criteria: Having Hyperprolactinemia, Hypothyroidism, Adrenal Insufficiency, Cushing's Disease and Diabetes Being in breastfeeding Taking Dopaminergic Drugs Taking hormonal druges for a month before entering the study History of hypersensitivity to herbal medicines Lack of drastic lifestyle changes in 4 areas: exercise, sleep, diet, patient excretion pattern (eg taking laxative ) from 2 weeks before the start of the study until the end of the study time

Design outcomes

Primary

MeasureTime frame
Number of menstrual cycles. Timepoint: At the beginning of the study (before the intervention), one month, two months and three months after the intervention and one month after the end of the intervention. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Acne. Timepoint: At the beginning of the study (before the intervention), one month, two months and three months after the intervention and one month after the end of the intervention. Method of measurement: GAGS Global Scoring System.;Hirsutism. Timepoint: At the beginning of the study (before the intervention), one month, two months and three months after the intervention and one month after the end of the intervention. Method of measurement: Freeman Galloway's table.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazieh Ghanbarian

Esfahan University of Medical Sciences

rgh1396@resident.mui.ac.ir+98 31 3266 5542

Outcome results

None listed

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