ID
38416
Descrizione
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 at the Follow-up Visit (Visit 3) on Day 30 +/- 2 or can be used for the last contact information.
collegamento
https://clinicaltrials.gov/ct2/show/NCT00038961
Keywords
versioni (1)
- 16/10/19 16/10/19 -
Titolare del copyright
GlaxoSmithKline
Caricato su
16 ottobre 2019
DOI
Per favore, per richiedere un accesso.
Licenza
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
Follow-Up
- StudyEvent: ODM
Descrizione
Follow-Up Record Day 30 ± 2 or Last Contact Information
Alias
- UMLS CUI-1
- C1522577
- UMLS CUI-2
- C1517741
- UMLS CUI-3
- C0332158
Descrizione
Type of Follow-Up contact
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C1522577
- UMLS CUI [1,2]
- C0332158
- UMLS CUI [1,3]
- C0332307
Descrizione
Follow-Up contact made by
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C1522577
- UMLS CUI [1,2]
- C1705415
Descrizione
Follow-Up contact with
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C1522577
- UMLS CUI [1,2]
- C0332158
Similar models
Follow-Up
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,2])
C1517741 (UMLS CUI-2)
C0332158 (UMLS CUI-3)
C0332158 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
C1705415 (UMLS CUI [1,2])