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To evaluate the effect of a Persian medicine product, containing silk, on the incidence of pregnancy in infertile women with polycystic ovary syndrom

To evaluate the effect of a Persian medicine product, containing silk, on the incidence of pregnancy in infertile women with polycystic ovary syndrome-A Randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221009056122N1
Enrollment
58
Registered
2022-11-01
Start date
2022-11-22
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Infertility in women with polycystic ovary syndrome. Female infertility associated with anovulation

Interventions

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Infertile women suffering from polycystic ovary syndrome referred to Rehane Infertility Center, Nekoui Hospital, Qom. Informed consent to enter the plan The period of infertility is at least 1 year and at most 5 years BMI less than 30 kg/m2

Exclusion criteria

Exclusion criteria: Male factor Infertility Tubular infertility other types of ovarian cysts except for PCO Endometriosis Premature ovarian failure (POF) and decreased ovarian reserve (DOR) Underlying and systemic disease and malignancy Breast diseases such as breast cysts Liver, kidney, joint and rheumatic disorders Other diseases including metabolic diseases such as diabetes and endocrine disorders including uncontrolled hypothyroidism, hyperprolactinemia, and Cushing's disease Breast diseases such as breast cysts Liver, kidney, joint and rheumatic disorders Other diseases including metabolic diseases such as diabetes and endocrine disorders including uncontrolled hypothyroidism, hyperprolactinemia, and Cushing's disease Other diseases include metabolic diseases such as diabetes and endocrine disorders including uncontrolled hypothyroidism, hyperprolactinemia, and Cushing's disease

Design outcomes

Primary

MeasureTime frame
Chemical pregnancy. Timepoint: After the first delay in menstruation, the fourth week of the menstruation cycle. Method of measurement: Serum ?-hCG meausurment.

Secondary

MeasureTime frame
Clinical pregnancy. Timepoint: After a positive serum ?-hCG test, the fifth to sixth week of the menstruation cycle. Method of measurement: Observing fetal heart rate on ultrasound.;The level of anxiety. Timepoint: The beginning and end of the intervention. Method of measurement: Anxiety score in Beck's questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBatoul Khayatzadeh

Ghoum University of Medical Sciences

bkhaiatzadeh@muq.ac.ir+98 25 3776 4073

Outcome results

None listed

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