Maternal and fetal haemodynamic response to Nifedipine tocolysis in normotensive pregnant women. - CORCA I

• Conditions: A more detailed investigation of the haemodynamic effect on the mother and fetus of Nifedipine tocolysis . Tocolysis will be used to facilitate external cephalic version for breech presentation at term.; MedDRA version: 9.1Level: LLTClassification code 10006356Term: Breech presentation; MedDRA version: 9.1Level: LLTClassification code 10048773Term: Tocolysis; MedDRA version: 9.1Level: LLTClassification code 10013596Term: Doppler ultrasound; MedDRA version: 9.1Level: LLTClassification code 10053094Term: Doppler echocardiography

• Registration Number: EUCTR2007-000467-23-NL
• Lead Sponsor: Erasmus MC

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2007-02-15
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

normotensive term singleton pregnancy
fetus in breech presentation
opted for external cephalic version
tocolysis with Nifedipine
Are the trial subjects under 18? yes
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)
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

contraindication for external cephalic version
contraindication for vaginal delivery
contraindication for nifedipine
cardiac disease

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified