Medical abortion in first and second trimester. (Induced) termination of pregnancy with unspecified complications
Conditions
Interventions
Intervention 1: Control group: Control group: In the control group, to prepare the cervix, 400 micrograms of misoprostol will be placed vaginally by a gynecologist 4 hours before surgery. Mesoprostol
Sponsors
Karaj University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age over 18 years for mothers Less or equal pregnancy age 24 weeks based on (LMP) and ultrasound of the first 3 months of pregnancy Patient satisfaction to participate in the study Legal permission for abortion is from the relevant authorities
Exclusion criteria
Exclusion criteria: Patients under 18 years of age Contraindications to the use of misoprostol (drug allergy, active asthma, heart disease, renal failure or glaucoma) Active genital infection Structural disorders of the uterus and bladder Cervical cancer History of cervical surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cervical dilatation rate. Timepoint: Before surgery and after general anesthesia. Method of measurement: Examination by a specialist.;Feeling sick. Timepoint: Before surgery and after general anesthesia. Method of measurement: Examination by a specialist doctor based on a five-digit criterion (without discomfort, with discomfort, relatively uncomfortable, very uncomfortable, unbearable).;Servicing preparation time. Timepoint: After receiving the drug until the start of surgery. Method of measurement: Examination by a specialist. | — |
Secondary
| Measure | Time frame |
|---|---|
| Side effects( include vaginal pain, pressure on the bladder, diarrhea and vaginal bleeding, and incomplete miscarriage.). Timepoint: Before general anesthesia, after the procedure and the patient regained consciousness. Method of measurement: Examination by a specialist doctor, ultrasound (if you have symptoms in favor of incomplete abortion once before discharge).;Cervical consistency. Timepoint: Before surgery and after general anesthesia. Method of measurement: Examination by a specialist doctor based on three-digit criteria (according to the surgeon, soft, medium, hard). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBita Badehnoosh
Karaj University of Medical Sciences
Outcome results
None listed