Home | All trials

[RDF data]
Trial NCT00187369

Resource URI: http://static.linkedct.org/resource/trials/NCT00187369
PropertyValue
linkedct:brief_title The Twin Birth Study: A Trial Comparing Planned Vaginal Birth to Elective Caesarean Section of Twins
linkedct:collaborator_agency <http://static.linkedct.org/resource/collabagency/1060>
linkedct:condition <http://static.linkedct.org/resource/condition/13319>
linkedct:criteria Inclusion Criteria: 1. Women at 32 0/7 - 38 6/7 weeks gestation 2. Estimated fetal weight of each fetus 1500 - 4000 g 3. Both twins alive at time of randomization 4. Twin A is in cephalic position Exclusion Criteria: 1. Monoamniotic twins 2. Lethal fetal anomaly of either fetus 3. Contraindication to labour or vaginal delivery for either twin 4. Previous participation in the Twin Birth Study
linkedct:description For twin pregnancies of 32-38 weeks gestation, where twin A is presenting cephalic, does a policy of planned CS decrease the likelihood of perinatal or neonatal mortality or serious neonatal morbidity, during the first 28 days after birth, compared to a policy of planned VB?
linkedct:download_date Information obtained from ClinicalTrials.gov on December 30, 2009
linkedct:eligibility_gender Female
linkedct:eligibility_healthy_volunteers No
linkedct:eligibility_maximum_age 45 Years
linkedct:eligibility_minimum_age 15 Years
linkedct:end_date December 2013
linkedct:enrollment 2800 (xsd:int)
linkedct:firstreceived_date September 12, 2005
linkedct:has_dmc Yes
linkedct:id NCT00187369
rdfs:label Trial NCT00187369
linkedct:lastchanged_date February 6, 2009
linkedct:lead_sponsor_agency Sunnybrook Health Sciences Centre
linkedct:location <http://static.linkedct.org/resource/location/20372>
linkedct:nct_id NCT00187369
linkedct:number_of_arms 2 (xsd:int)
linkedct:number_of_groups 0 (xsd:int)
linkedct:official_title The Twin Birth Study: A Multicentre Randomised Controlled Trial Comparing Planned Vaginal Birth to Elective Caesarean Section of Twins More Than or Equal to 32 Weeks Gestation
linkedct:org_study_id MCT-63164
linkedct:overall_contact_email jon.barrett@sw.ca
linkedct:overall_contact_last_name Jon F Barrett
linkedct:overall_contact_phone 416-351-2533
linkedct:overall_official <http://static.linkedct.org/resource/overall_official/29626>
linkedct:overall_status Recruiting
linkedct:oversight <http://static.linkedct.org/resource/oversight/402>
foaf:page <http://clinicaltrials.gov/show/NCT00187369>
linkedct:phase N/A
linkedct:primary_completion_date December 2011
linkedct:primary_outcomes <http://static.linkedct.org/resource/primary_outcomes/39261>
linkedct:secondary_id ISRCTN74420086
linkedct:secondary_outcomes <http://static.linkedct.org/resource/secondary_outcomes/34250>
linkedct:secondary_outcomes <http://static.linkedct.org/resource/secondary_outcomes/88344>
linkedct:source Sunnybrook Health Sciences Centre
linkedct:start_date December 2003
linkedct:study_design Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety Study
linkedct:study_type Interventional
linkedct:summary For twin pregnancies at 32-38 weeks gestation, where twin A is head down, does a policy of planned caesarean section (CS) lower the likelihood of death or serious illness, during the first 28 days after birth, compared to a plan for vaginal birth (VB)?
rdf:type linkedct:trials
linkedct:verification_date February 2009