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The Effect of evening primrose oil on Fertility outcomes in the women undergoing IVF treatment.

Phase 2
Recruiting
Conditions
Infertility.
Female infertility
Registration Number
IRCT20110606006709N21
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
84
Inclusion Criteria

Women with primary and secondary infertility are candidates for IVF
Women 20-40 years
Women with a BMI between 18.5 and 29.9

Exclusion Criteria

Follow a specific dietary pattern for medical or other reasons
History of seizures
Malignancy
Use of chemotherapy and radiotherapy or history of use corticosteroid drugs for up to one month
Continuous and daily consumption of herbal yeas (borage ...)
Tobacco and alcohol or any drug abuse
IVF cycle = 4
Use of donated sperm or egg or frozen sperm and egg
sever endometriosis
Having uterine anomalies
Use of blood thinners

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Implantation rate. Timepoint: at week 5 of pregnancy will be calculated. Method of measurement: The implantation rate will be calculated by dividing the number of sacs visible in the ultrasound by the number of embryos transferred.;Fertility rate. Timepoint: One day after the IVF procedure will be determined. Method of measurement: Fertility rate It will be calculated as the number of fertilized oocytes divided by the total number of oocytes removed.
Secondary Outcome Measures
NameTimeMethod
Fetal quality status. Timepoint: On the third day after will be determined fertilization. Method of measurement: Third day, fetal quality under the microscope will be determined by an experienced person according to the fetal quality grading chart.;Pregnancy Test Status. Timepoint: 14 days after embryo transfer will be determined. Method of measurement: Clinical pregnancy as positive for blood ßHCG test will be specified.;Side Effects evening primrose oil supplementation. Timepoint: During the study will be reported. Method of measurement: By completing the checklist of side effects will be obtained.
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