Ignite Creation Date:
2024-05-05 @ 5:19 PM
Last Modification Date:
2024-10-26 @ 9:30 AM
Study NCT ID:
NCT00432250
Status:
COMPLETED
Last Update Posted:
2007-02-07
First Post:
2007-02-06
Brief Title:
The Use of Cervical Length to Reduce Hospital Stay in Women Admitted Because of Preterm Labor
Sponsor:
Hospital Clinic of Barcelona
Organization:
Hospital Clinic of Barcelona
Study Overview
Official Title:
None
Status:
COMPLETED
Status Verified Date:
2007-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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
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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None