Thromboelastography to Assess Hemostatic Changes in Patients Undergoing Elective Cesarean Delivery. [clinicaltrials:NCT00767832]
Thromboelastography to Assess Hemostatic Changes in Patients Undergoing Elective Cesarean Delivery. [clinicaltrials:NCT00767832]
Bio2RDF identifier
NCT00767832
Bio2RDF namespace
clinicaltrials
Bio2RDF uri
http://bio2rdf.org/clinicaltrials:NCT00767832
identifiers.org URI
anticipated enrollment [clinicaltrials_vocabulary:anticipated-enrollment]
authority [clinicaltrials_vocabulary:authority]
biospec retention [clinicaltrials_vocabulary:biospec-retention]
None Retained
biospec_descr [clinicaltrials_vocabulary:biospec_descr]
Venous blood
brief summary [clinicaltrials_vocabulary:brief-summary]
The purpose of the stud ...... ated to estimated blood loss.
brief title [clinicaltrials_vocabulary:brief-title]
Thromboelastography to Assess ...... ng Elective Cesarean Delivery.
clinicaltrials_vocabulary:primary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:primary-outcome]
clinicaltrials_vocabulary:secondary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:secondary-outcome]
completion date [clinicaltrials_vocabulary:completion-date]
2009-06-01T00:00:00Z
condition [clinicaltrials_vocabulary:condition]
country [clinicaltrials_vocabulary:country]
detailed description [clinicaltrials_vocabulary:detailed-description]
The purpose of the stud ...... ated to estimated blood loss.
download date [clinicaltrials_vocabulary:download-date]
ClinicalTrials.gov processed this data on August 10, 2015
eligibility [clinicaltrials_vocabulary:eligibility]
firstreceived date [clinicaltrials_vocabulary:firstreceived-date]
2008-10-03T00:00:00Z
has expanded access [clinicaltrials_vocabulary:has-expanded-access]
intervention browse [clinicaltrials_vocabulary:intervention-browse]
is fda regulated [clinicaltrials_vocabulary:is-fda-regulated]
lastchanged date [clinicaltrials_vocabulary:lastchanged-date]
2009-11-06T00:00:00Z
lead sponsor [clinicaltrials_vocabulary:lead-sponsor]
location [clinicaltrials_vocabulary:location]
nct id [clinicaltrials_vocabulary:nct-id]
NCT00767832
number of arms [clinicaltrials_vocabulary:number-of-arms]
official title [clinicaltrials_vocabulary:official-title]
Thromboelastography to Assess ...... ng Elective Cesarean Delivery.
org study id [clinicaltrials_vocabulary:org-study-id]
SU-08252008-1287
overall official [clinicaltrials_vocabulary:overall-official]
overall status [clinicaltrials_vocabulary:overall-status]
oversight [clinicaltrials_vocabulary:oversight]
primary completion date [clinicaltrials_vocabulary:primary-completion-date]
2009-06-01T00:00:00Z
responsible party [clinicaltrials_vocabulary:responsible-party]
secondary id [clinicaltrials_vocabulary:secondary-id]
source [clinicaltrials_vocabulary:source]
start date [clinicaltrials_vocabulary:start-date]
2008-08-01T00:00:00Z
study design [clinicaltrials_vocabulary:study-design]
study type [clinicaltrials_vocabulary:study-type]
url [clinicaltrials_vocabulary:url]
verification date [clinicaltrials_vocabulary:verification-date]
2009-11-01T00:00:00Z
identifier
clinicaltrials:NCT00767832
title
Thromboelastography to Assess ...... ng Elective Cesarean Delivery.
@en
type
label
Thromboelastography to Assess ...... . [clinicaltrials:NCT00767832]
@en