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Clinical Trials/IRCT20180227038892N1
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

Iran University of Medical Sciences0 sites60 target enrollmentStarted: TBDLast updated:
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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