Clinical Trials Directory

Trials / Completed

CompletedNCT00432250

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

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
150 (planned)
Sponsor
Hospital Clinic of Barcelona · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers

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.

Conditions

Interventions

TypeNameDescription
PROCEDURECervical length ultrasound

Timeline

Start date
2002-01-01
Completion
2005-04-01
First posted
2007-02-07
Last updated
2007-02-07

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT00432250. Inclusion in this directory is not an endorsement.