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The Use of Cervical Length to Reduce Hospital Stay in Women Admitted Because of Preterm Labor.

Phase 4
Completed
Conditions
Labor, Premature
Cervical Length
Registration Number
NCT00432250
Lead Sponsor
Hospital Clinic of Barcelona
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
150
Inclusion Criteria
  • Admitted because of preterm labor
  • Not delivered after 24-48 h of admission
  • Single pregnancy
  • Intact membranes
  • Gestational age between 24.0 and less tahn 36.0 weeks
  • Bishop score < 6
Exclusion Criteria
  • Fetal death or malformation
  • Signs of chorioamnionitis
  • Non-reassuring fetal test

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Length of hospital stay
Gestational age at delivery
Secondary Outcome Measures
NameTimeMethod
Rate of hospital stay below 3 days
Interval admission-to-delivery < 7 days
Rate of preterm delivery before 37 weeks
Rate of preterm delivery before 34 weeks

Trial Locations

Locations (1)

Hospital Clínic of Barcelona

🇪🇸

Sabino de Arana 1, Barcelona, Spain

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