ID
38091
Beskrivning
Study ID: 103414 Clinical Study ID: 103414 Study Title: A Multicenter, Randomized, Double-blind, Parallel Group Trial to Demonstrate the Efficacy of Fondaparinux Sodium in Association With Intermittent Pneumatic Compression (IPC) Versus IPC Used Alone for the Prevention of Venous Thromboembolic Events in Subjects at Increased Risk Undergoing Major Abdominal surgery Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00038961 https://clinicaltrials.gov/ct2/show/NCT00038961 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: Fondaparinux Sodium Trade Name: Fondaparinux Sodium Study Indication: Thrombosis This phase III placebo-controlled trial studies the efficacy and safety of Fondaparinux as an additional prevention measure of venous thromboembolic events (VTE) in patients above the age of 40 with intermediate or high VTE risk undergoing abdominal surgery. The study consists of a Screening Visit (Visit 0), the baseline visit on Day 1, the day of the surgery (Visit 1), the treatment period (denoted in its entirety as Visit 2) consisting of administration of Fondaparinux (2.5mg subcutaneously once daily) or placebo starting on Day 1 and continuing at least up to Day 5, possibly up to Day 9, in parallel to intermittent pneumatic compression and possibly elastic stockings, followed by a mandatory bilateral venography no longer than 24 hours after study drug cessation, and finally a Follow-up Visit (Visit 3) on Day 30 +/- 2. This form contains basic information on whether and when the subject has been discharged from hospital, and is to be filled in at the end of Visit 2 or at Visit 3.
Länk
https://clinicaltrials.gov/ct2/show/NCT00038961
Nyckelord
Versioner (1)
- 2019-09-16 2019-09-16 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
16 september 2019
DOI
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Licens
Creative Commons BY-NC 3.0
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Fondaparinux in Addition to Intermittent Pneumatic Compression in Abdominal Surgery Patients at VTE Risk - NCT00038961
Discharge Information
- StudyEvent: ODM
Beskrivning
Discharge
Alias
- UMLS CUI-1
- C0030685
Beskrivning
Record either Date of discharge OR select "Patient still hospitalized at last contact or death during the first hospitalization."
Datatyp
date
Alias
- UMLS CUI [1]
- C2361123
Beskrivning
Record either Date of discharge OR select "Patient still hospitalized at last contact or death during the first hospitalization."
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0019993
- UMLS CUI [1,2]
- C0549178
- UMLS CUI [1,3]
- C0805839
- UMLS CUI [2,1]
- C0011065
- UMLS CUI [2,2]
- C0347984
- UMLS CUI [2,3]
- C0205435
- UMLS CUI [2,4]
- C0019993
Similar models
Discharge Information
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0805839 (UMLS CUI [1,3])
C0011065 (UMLS CUI [2,1])
C0347984 (UMLS CUI [2,2])
C0205435 (UMLS CUI [2,3])
C0019993 (UMLS CUI [2,4])