Medical abortion. Complications following (induced) termination of pregnancy
Conditions
Interventions
Intervention 1: Intervention group: Embedding of Laminaria In the cervix with 400 µg Misoprostol Vaginally every 8 hours, up to 48 hours. Intervention 2: Control group: 400 µg Misoprostol Vaginally ev
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Pregnant women between 14-20 weeks of pregnancy at Imam Ali Hospital who are candidates for termination of pregnancy due to severe anomalies or due to fetal death Singleton conditions, parity 1 to 3, painless and uterine infections
Exclusion criteria
Exclusion criteria: Allergy to the drug parity of more than three severe anemia active liver disease cardiovascular disease uncontrolled seizures having IUD Placenta Previa History of cesarean section previous incision on the uterus Use of corticosteroids Use of anti coagulants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Termination of pregnancy. Timepoint: Every eight hours to six times. Method of measurement: dilatation of cervix and contraction. | — |
Secondary
| Measure | Time frame |
|---|---|
| Need for curettage. Timepoint: From the start, every eight hours to six turns. Method of measurement: Clinical examinations.;Abortion time in labor. Timepoint: Interval between administration of drug and expulsion of fetus. Method of measurement: Record time.;Time of admission in hospital after abortion. Timepoint: From the time of the abortion to the patient's discharge. Method of measurement: Record time. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Behnood
Zahedan University of Medical Sciences
Outcome results
None listed