Infertility and implantation problems. Pregnancy with abortive outcome
Conditions
Interventions
Intervention 1: The intervention group received a dose of 400 IU vitamin E Zahravi purchased from pharmaceutical companies and patients given take a number of the drug every day for three months. Brie
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
25 Years to 36 Years
Inclusion criteria
Inclusion criteria: Women with implantation problem Age range of 25–36 years old
Exclusion criteria
Exclusion criteria: Having an abnormal uterus Having a polycysticovary syndrome Glucose intolerance Thyroid disease Having autoimmune diseases or cancer Smoking The lack of intention to continue cooperationin the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endometrial thickness. Timepoint: Beginning of the study and three months later. Method of measurement: By vaginal ultrasound. | — |
Secondary
| Measure | Time frame |
|---|---|
| Malondialdehyde. Timepoint: Beginning of the study and three months later. Method of measurement: Spectrophotometry.;Vitamin E. Timepoint: Beginning of the study and three months later. Method of measurement: ELISA kit.;Follicle-stimulating hormone. Timepoint: Beginning of the study and three months later. Method of measurement: ELISA kit.;Luteinizing hormone. Timepoint: Beginning of the study and three months later. Method of measurement: ELISA kit.;Estradiol (. Timepoint: Beginning of the study and three months later. Method of measurement: ELISA kit.;Progesterone. Timepoint: Beginning of the study and three months later. Method of measurement: ELISA kit.;Vascular endothelial growth factor. Timepoint: Beginning of the study and three months later. Method of measurement: PCR.;Oxidized low-density lipoprotein (Ox-LDL). Timepoint: Beginning of the study and three months later. Method of measurement: PCR.;Interleukin-1. Timepoint: Beginning of the study and three months later. Method of measurement: PCR.;Interleukin-6. Timepoint: Beginning of the study and three months later. Method of measurement: PCR.;Interleukin-8. Timepoint: Beginning of the study and three months later. Method of measurement: PCR.;Tumor necrosis factor alpha. Timepoint: Beginning of the study and three months later. Method of measurement: PCR. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. E. Aghadavood Jolfaee
Kashan University of Medical Sciences
Outcome results
None listed