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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Cervical 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.