Statistical tests: *Chi‐square test; **Mann‐Whitney Before discharge, the primary outcome was assessed based on the proportion of women remaining undelivered during the whole period of hospitalisation. Medications were continued for 48–72 hours.The percentage of women who remained undelivered during hospitalisation.From January 2015 to November 2016, 239 women were randomised. For Adult. The usual dosage is three times daily based on maximum median plasma concentrations reached within 60 minutes and a half‐life of 4 hours,Regarding the safety of SC, although no deleterious effects were seen among babies after delivery, there was no long‐term follow up. Statistical tests: *Chi‐square test; **Mann‐Whitney Statistical tests: *Mann‐Whitney 2014 Jul 11;(7):CD006169. Statistical tests: *Chi‐square test; **Mann‐Whitney Statistical tests: *Chi‐square test; **Mann‐Whitney Please enable it to take advantage of the complete set of features!
doi: 10.1002/14651858.CD011200.pub2. Epub 2019 Feb 17.J Obstet Gynaecol. Statistical tests: *Chi‐square test; **Mann‐Whitney National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implicationsImplications of idiopathic preterm delivery for previous and subsequent pregnanciesPlacental vascular pathology findings and pathways to preterm deliverythe European Association of Perinatal Medicine‐Study Group on ‘Preterm Birth’Guidelines for the management of spontaneous preterm laborCalcium channel blockers for inhibiting preterm labour; a systematic review of the evidence and a protocol for administration of nifedipineNifedipine for the management of preterm labor: a systematic review and metanalysisInhibition of neuroeffector transmission in human vas deferens by sildenafilInvolvement of a nitric oxide‐cyclic guanosine monophosphate pathway in control of human uterine contractility during pregnancyACOG practice bulletin no. Statistical tests: *Chi‐square test; **Mann‐Whitney doi: 10.1002/14651858.CD002255.pub2.Cochrane Database Syst Rev. All authors contributed to the interpretation of the data and manuscript preparation.This study has been approved by the ethics committee of the Menoufia University Hospitals, Shebin El‐Kom, Egypt (OB/GYN protocols, November 2014).
Its main use until now has been in the management of hypertension and angina.
Cases included those presenting at the outpatient clinic or emergency room and those referred from other hospitals.Preterm labour was defined based on contraction frequency (persistence of at least two symptomatic uterine contractions within a 10‐minute period during 60 minutes’ observation) and cervical changes (cervical dilation between 0 and 3 cm for nulliparous and between 1 and 3 cm for multiparous, with cervical effacement <50%).Exclusion criteria were: multiple pregnancy, advanced cervical dilation (>4 cm) with or without membranes bulging into the vagina, ruptured fetal membranes, suspected chorioamnionitis (unexplained fetal tachycardia or maternal temperature >38°C), contraindication for nifedipine and/or SC therapy, a major chronic medical disorder (such as chronic hypertension, chronic renal disease, and pregestational diabetes mellitus, as these conditions would increase the risk of PTL and potentially confound the primary study outcome) and general contraindications to tocolytic therapy.Women were randomly assigned in a 1:1 ratio to two study groups using a computerised random number table generator to obtain a trial sequence which was hidden in sealed numbered opaque envelopes prepared by the medical research officer in the hospital. Statistical tests: *Mann‐Whitney Clipboard, Search History, and several other advanced features are temporarily unavailable. Epub 2020 Mar 5.BJOG.
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