infertile women due to poly cystic ovary syndrome.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Married women with infertility with definitive diagnosis of polycystic ovary syndrome based on Rotterdam criteria by gynecologists Lack of known mental illnesses under treatment Do not use psychotropic drugs and narcotics Married women Ability to read, write and speak Persian Do not attend counseling sessions or medication for fertility Couples agree to have vaginal sex (for example, two to three times a week) around the time of ovulation during the time of the study No endometrial cancer or cervical cancer The subject should not have a history of deep vein thrombosis or pulmonary embolism
Exclusion criteria
Exclusion criteria: ?Endocrine, endogenous or any chronic diseases affecting the rate of fertilization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fertility Quality of Life. Timepoint: participants completed the FertiQol questionnaire before the intervention and three months after the end of the intervention. Method of measurement: FertiQol questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Conception success. Timepoint: At four times: immediately after the end of treatment, one month, two months, three months after the end of treatment in case of delay in menstruation. Method of measurement: Quality Beta-HCG by blood sample. | — |
Countries
Iran (Islamic Republic of)
Contacts
Kerman University of Medical Sciences