IRCT20180227038892N1Recruiting未知
Comparison effect of oral Dydrogesterone on the treatment of preterm labor with oral Nifedipine in pregnant women admitted with a diagnosis of risk of preterm labor
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 45 years (—)
- Sex
- Female
Inclusion Criteria
- •A total of 60 women aged 18-45 years with a singleton pregnancy of 26-34 weeks, admitted with a diagnosis of preterm labor, are included in the study.
Exclusion Criteria
- •Exclusion criteria include any maternal or fetal conditions that require immediate delivery (including fetal distress; placenta abruption; chorioamnionitis; severe preeclampsia; Patients who have entered the active phase of labor ( cervical dilatation>=4cm); vaginal bleeding; Ruptured of membrane; Uterine distention for example due to multiple pregnancy and polyhydramnios; The presence of any systemic infection; Fever greater than 38 degrees Centigrade; Intrauterine growth restriction; Blood pressure above 140/90 mm Hg; Fetal anomalies; Contraindications to the use of tocolytics, history of any allergy to progesterone and a history of any thromboembolic disease.
Investigators
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