ID
38086
Descripción
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 information on the adjudication of any death occuring during the study.
Link
https://clinicaltrials.gov/ct2/show/NCT00038961
Palabras clave
Versiones (1)
- 16/9/19 16/9/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
16 de septiembre de 2019
DOI
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Licencia
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
Death Adjudication
- StudyEvent: ODM
Descripción
Death Adjudication Form
Alias
- UMLS CUI-1
- C0680730
- UMLS CUI-2
- C0011065
Descripción
Classification Status
Alias
- UMLS CUI-1
- C0008902
Descripción
Adjudicators
Alias
- UMLS CUI-1
- C0401783
Descripción
Adjudicator Signature 1
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0401783
- UMLS CUI [1,2]
- C1519316
Descripción
Adjudicator Signature 2
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0401783
- UMLS CUI [1,2]
- C1519316
Descripción
Date of adjudication
Tipo de datos
text
Alias
- UMLS CUI [1]
- C4740194
Similar models
Death Adjudication
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,2])
C0011065 (UMLS CUI-2)
C1516308 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C1519316 (UMLS CUI [1,2])
C1519316 (UMLS CUI [1,2])