IRCT2017072326695N2CompletedPhase 3
Evaluation of the results of using 25 µg sublingual misoprostol and Foley catheter together and each one alone in preparing cervix in low-term term pregnancies for termination of pregnancy with less than 4
Vice chancellor for research, Tehran University of Medical Science0 sites99 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- Enrollment
- 99
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 45 years (—)
- Sex
- Female
Inclusion Criteria
- •Pregnant women who indicate a termination of pregnancy (37-42 weeks); have normal delivery conditions: Cephalic presentation; women aged 18-45; urine score less than 4
- •Exclusion criteria: Abnormal heartbeat; Vaginal bleeding; Placenta praevia & Placental abruption; Multiple birth; Non-Cephalic presentation & Macrosomia; Infertility history greater than or equal to 6 years old and abnormal or fetal death;
- •Multi-frequency higher than most 7; Rupture of Membeans; Intrauterine growth restriction and weighing over 4000 grams; History of uterine surgeries; tachycardia in mother; Preeclampsia; Abnormal liver and kidney tests
Exclusion Criteria
- Not provided
Investigators
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