medical abortion. Medical abortion
Conditions
Interventions
Intervention 1: Control group: Group A patients in whom abortion will be performed with vaginal and oral misoprostol are given two 200 µg misoprostol tablets orally (sublingually) and two vaginally in
Sponsors
Dezfoul University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Hemoglobin level greater than 10 gr / l Diastolic pressure less than 95 mmhg Serum hcg level less than 3000 iu / l Gestational age less than 14 weeks
Exclusion criteria
Exclusion criteria: Use of abortion drugs in the last three months itching during pregnancy Existence of adrenal disorders Porphyria, steroid-related cancer, acute or chronic liver disease or thromboembolism History of chronic lung diseases such as asthma, bronchitis, bronchiectasis known allergy to letrozole or misoprostol Breast feeding Multipfetal pregnancy More than two previous cesarean sections uterine surgery and myomectomy contraindications to the letrozol and mosoprostol Existence of intrauterine devices (IUD) Uncontrolled seizures Coagulation disorder or use of anticoagulants Active liver disease, cardiovascular disease Adrenal disease Consumption of glucocorticoids
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fetus abortion. Timepoint: Before and after abortion. Method of measurement: Eight hours after the intervention, and every twenty-four hours up to three days if the abortion doesn't occur. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactvahid.kheirandish
Dezfoul University of Medical Sciences
Outcome results
None listed