EUCTR2008-005987-15-NL
Active, not recruiting
Not Applicable
Preventing preterm birth: Costs and effects of screening of healthy women with a singleton pregnancy for a short cervical length. - The Triple P study
AMC Amsterdam0 sitesOctober 30, 2008
DrugsUtrogestan
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- AMC Amsterdam
- Status
- Active, not recruiting
- Last Updated
- 14 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\-\- Capacitated women
- •\-\- \= 18 years old
- •\-\- Singleton healthy pregnancy
- •\-\- Two times a cervical length \= 25 mm: a cervical length \= 25 mm at 16\-20 weeks gestation, and a confirmation of this result with a repeat measurement of the cervical length at 20\-22 weeks gestation
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) no
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Women with a pregnancy with major foetal abnormalities, painful regular uterine contractions, a history of ruptured membranes or a cervical cerclage will be excluded. In addition, women with a previous preterm birth are excluded as well.
Outcomes
Primary Outcomes
Not specified
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