ID
38586
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 is to be filled in if an autopsy has been performed.
Link
https://clinicaltrials.gov/ct2/show/NCT00038961
Palabras clave
Versiones (2)
- 17/10/19 17/10/19 -
- 25/10/19 25/10/19 - Sarah Riepenhausen
Titular de derechos de autor
GlaxoSmithKline
Subido en
25 de octubre de 2019
DOI
Para solicitar uno, por favor iniciar sesión.
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
Autopsy Form
- StudyEvent: ODM
Descripción
Autopsy Form
Alias
- UMLS CUI-1
- C0004398
Descripción
If yes, complete form.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0004398
Descripción
Date of Autopsy
Tipo de datos
date
Alias
- UMLS CUI [1]
- C3864942
Descripción
If yes, specify location
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0034065
Descripción
Pulmonary Embolism in Left pulmonary artery
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C0226069
Descripción
Pulmonary Embolism in Right pulmonary artery
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C0226054
Descripción
Pulmonary Embolism in Left lobar arteries
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C0503867
- UMLS CUI [1,3]
- C0205091
Descripción
Pulmonary Embolism in Right lobar arteries
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C0503867
- UMLS CUI [1,3]
- C0205090
Descripción
Pulmonary Embolism in Left segmental arteries
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C0503402
- UMLS CUI [1,3]
- C0205091
Descripción
Pulmonary Embolism in Right segmental arteries
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C0503402
- UMLS CUI [1,3]
- C0205090
Descripción
Pulmonary Embolism in Main pulmonary trunk
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C2954153
Descripción
If yes, specify location
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0149871
Descripción
Deep Vein Thrombosis in Left calf
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0230445
- UMLS CUI [1,3]
- C0205091
Descripción
Deep Vein Thrombosis in Right calf
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0230445
- UMLS CUI [1,3]
- C0205090
Descripción
Deep Vein Thrombosis in Left popliteal vein
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0835016
Descripción
Deep Vein Thrombosis in Right popliteal vein
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0835015
Descripción
Deep Vein Thrombosis in Left femoral vein
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0739301
Descripción
Deep Vein Thrombosis in Right femoral vein
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0739300
Descripción
Deep Vein Thrombosis in Left iliac vein
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C4520258
Descripción
Deep Vein Thrombosis in Right iliac vein
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C4520257
Descripción
Deep Vein Thrombosis in Inferior vena cava
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0149871
- UMLS CUI [1,2]
- C0042458
Descripción
If yes, specify
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0042487
- UMLS CUI [2,1]
- C0151942
- UMLS CUI [2,2]
- C0205394
Descripción
if applicable
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1521902
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0042487
- UMLS CUI [2,1]
- C1521902
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [2,3]
- C0151942
Descripción
if yes specify
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0019080
Descripción
if applicable
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0019080
- UMLS CUI [1,2]
- C1521902
Descripción
if yes specify
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1335151
Descripción
if applicable
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1521902
- UMLS CUI [1,2]
- C1335151
Descripción
Investigator's signature
Alias
- UMLS CUI-1
- C2346576
Descripción
"I, the undersigned, certify that I have carefully examined all entries on the CRF for this subject.To the best of my knowledge, all information is correct."
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2346576
Descripción
Investigator's signature date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Similar models
Autopsy Form
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,2])
C0226069 (UMLS CUI [1,2])
C0226054 (UMLS CUI [1,2])
C0503867 (UMLS CUI [1,2])
C0205091 (UMLS CUI [1,3])
C0503867 (UMLS CUI [1,2])
C0205090 (UMLS CUI [1,3])
C0503402 (UMLS CUI [1,2])
C0205091 (UMLS CUI [1,3])
C0503402 (UMLS CUI [1,2])
C0205090 (UMLS CUI [1,3])
C2954153 (UMLS CUI [1,2])
C0230445 (UMLS CUI [1,2])
C0205091 (UMLS CUI [1,3])
C0230445 (UMLS CUI [1,2])
C0205090 (UMLS CUI [1,3])
C0835016 (UMLS CUI [1,2])
C0835015 (UMLS CUI [1,2])
C0739301 (UMLS CUI [1,2])
C0739300 (UMLS CUI [1,2])
C4520258 (UMLS CUI [1,2])
C4520257 (UMLS CUI [1,2])
C0042458 (UMLS CUI [1,2])
C0042487 (UMLS CUI [1,2])
C0151942 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C0205394 (UMLS CUI [1,2])
C0042487 (UMLS CUI [1,3])
C1521902 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C0151942 (UMLS CUI [2,3])
C1521902 (UMLS CUI [1,2])
C1335151 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
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