Assess Efficacy and Safety of TachoComb H vs. Standard Surgical Treatment (i.e. Suturing) in Patients Undergoing Prostatectomy (TC-017-AU) [clinicaltrials:NCT00290836]

Bio2RDF identifier

NCT00290836

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Bio2RDF namespace

clinicaltrials

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Bio2RDF uri

http://bio2rdf.org/clinicaltrials:NCT00290836

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identifiers.org URI

NCT00290836

authority [clinicaltrials_vocabulary:authority]

clinicaltrials_resource:e478999f19782873e6063cf7552726b8

brief summary [clinicaltrials_vocabulary:brief-summary]

The overall objective i ...... centration of drainage fluid.

http://www.w3.org/2001/XMLSchema#string

brief title [clinicaltrials_vocabulary:brief-title]

Assess Efficacy and Safety of ...... oing Prostatectomy (TC-017-AU)

http://www.w3.org/2001/XMLSchema#string

clinicaltrials_vocabulary:primary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:primary-outcome]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:94587505a379333c3d43de148ae69e81]

clinicaltrials_vocabulary:secondary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:secondary-outcome]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:3ed97f715636527f8b0bead8ea3de355]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:4f90c41a94e57339dd852ce0c48a1869]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:76f462ebbcbd946220f75135e86ac880]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:85432607825b7b5c1c35c52ab88fe638]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:8bd2caaecaafd4e1cdc04ced231b844b]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:9791532de192878f2c0eb0f24a32bfa3]

Efficacy: Is the percentage of patients/treatment group in which efficient intra-operative haemostasis is achieved within 10 minutes after applying test treatment according to randomisation after primary surgical haemostasis. [clinicaltrials_resource:a184b7e8526a7d215edd6d1550a73845]

completion date [clinicaltrials_vocabulary:completion-date]

2007-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

condition [clinicaltrials_vocabulary:condition]

Control of Local Bleeding in Patients Undergoing Prostatectomy. [clinicaltrials_resource:fbd69eb26c5d389fd27becca432e6378]

country [clinicaltrials_vocabulary:country]

Denmark [clinicaltrials_resource:424214945ba5615eca039bfe5d731c09]

download date [clinicaltrials_vocabulary:download-date]

ClinicalTrials.gov processed this data on August 10, 2015

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eligibility [clinicaltrials_vocabulary:eligibility]

eligibility for clinicaltrials:NCT00290836 [clinicaltrials_resource:1f077d33e21d1f32ac1bbaeede0ef1b0]

enrollment [clinicaltrials_vocabulary:enrollment]

120

http://www.w3.org/2001/XMLSchema#integer

firstreceived date [clinicaltrials_vocabulary:firstreceived-date]

2005-12-16T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

has expanded access [clinicaltrials_vocabulary:has-expanded-access]

No

http://www.w3.org/2001/XMLSchema#string

intervention [clinicaltrials_vocabulary:intervention]

Human fibrinogen/thrombin and bovine aprotinin (TachoComb H) [clinicaltrials_resource:dfb8cf807c8a59c1f3ebe26fab165bba]

is fda regulated [clinicaltrials_vocabulary:is-fda-regulated]

No

http://www.w3.org/2001/XMLSchema#string

lastchanged date [clinicaltrials_vocabulary:lastchanged-date]

2012-05-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

lead sponsor [clinicaltrials_vocabulary:lead-sponsor]

Nycomed [clinicaltrials_resource:2a1fdd2d1e9a927161504a5702f2ae5d]

location [clinicaltrials_vocabulary:location]

Nycomed [clinicaltrials_resource:6883d04f92026d8aceb26fc53efae4a6]

nct id [clinicaltrials_vocabulary:nct-id]

NCT00290836

http://www.w3.org/2001/XMLSchema#string

official title [clinicaltrials_vocabulary:official-title]

An Open, Randomised, Prospecti ...... ients Undergoing Prostatectomy

http://www.w3.org/2001/XMLSchema#string

org study id [clinicaltrials_vocabulary:org-study-id]

TC-017-AU

http://www.w3.org/2001/XMLSchema#string

start date [clinicaltrials_vocabulary:start-date]

2004-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

study design [clinicaltrials_vocabulary:study-design]

clinicaltrials:NCT00290836 study design [clinicaltrials_resource:01bda11442ff663b062d07efb7499cfd]

study type [clinicaltrials_vocabulary:study-type]

Interventional [clinicaltrials_resource:843ac00ae5d0b7c7defb84fb42c2ce31]

url [clinicaltrials_vocabulary:url]

NCT00290836

verification date [clinicaltrials_vocabulary:verification-date]

2012-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

identifier

clinicaltrials:NCT00290836

http://www.w3.org/2001/XMLSchema#string

title

Assess Efficacy and Safety of ...... oing Prostatectomy (TC-017-AU)

@en

inDataset

clinicaltrials_resource:bio2rdf.dataset.clinicaltrials.R3

type

Clinical Study [clinicaltrials_vocabulary:Clinical-Study]

clinicaltrials resource [clinicaltrials_vocabulary:Resource]

label

Assess Efficacy and Safety of ...... ) [clinicaltrials:NCT00290836]

@en