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The objective of this study was to investigate the effect of the use of sonographic cervical length (CL) on the hospital stay in women admitted because of preterm labor.
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Eligible women who agreed to participate in the study were randomized by means of a central randomization office into two groups:
CONTROL group: cervical length was measured but the result was blinded to the physician in charge and women was managed according to the standard protocol.
STUDY group: cervical length was measured and the result was reported to the physician in charge. If cervical length was of 25 mm or more, discharge in 12-24 h was recommended. If cervical length was less than 25 mm, decision on discharge was made following clinical criteria.
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Data sourced from clinicaltrials.gov
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