ID
38093
Description
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 medical/surgical history and risk factors for VTE assessed during the Screening Visit (Visit 0). This form can be filled in starting 30 days before the surgery, whereas the laboratory tests which also need to be performed during Screening have to be done in the 7 days before the surgery (in a different form).
Lien
https://clinicaltrials.gov/ct2/show/NCT00038961
Mots-clés
Versions (1)
- 16/09/2019 16/09/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
16 septembre 2019
DOI
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Licence
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
Medical/Surgical History, VTE Risk Factors
- StudyEvent: ODM
Description
Specific Medical History/Risk Factors for VTE
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0035648
- UMLS CUI-3
- C1861172
Description
DVT
Type de données
boolean
Alias
- UMLS CUI [1]
- C0149871
Description
Pulmonary Embolism
Type de données
boolean
Alias
- UMLS CUI [1]
- C0034065
Description
Stroke
Type de données
boolean
Alias
- UMLS CUI [1]
- C0038454
Description
Myocardial Infarction
Type de données
boolean
Alias
- UMLS CUI [1]
- C0027051
Description
Recent major surgery or trauma
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0679637
- UMLS CUI [1,3]
- C0332185
- UMLS CUI [2,1]
- C0262926
- UMLS CUI [2,2]
- C0332677
- UMLS CUI [2,3]
- C0332185
Description
If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C1882062
Description
present at study start for cancer present or treated within the last 6 months
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1882062
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0021390
Description
Inflammatory Bowel Disease present at study start
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0021390
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0024117
Description
Chronic Obstructive Pulmonary Disease present at study start
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0024117
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
Bed confinement during more than the three days preceding surgery If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0020944
Description
Bed confinement during more than the three days preceding surgery
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0020944
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0009905
Description
Oral contraceptive use present at study start
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0009905
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0042345
Description
Varicose veins present at study start
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0042345
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
Prothrombotic states or deficiencies of ATIII, deficiencies of or resistance to protein C or protein S, lupus anticoagulant, antiphospholipid antibody etc.. If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0398623
Description
Prothrombotic states or deficiencies of ATIII, deficiencies of or resistance to protein C or protein S, lupus anticoagulant, antiphospholipid antibody etc..
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0398623
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
If yes, answer next question
Type de données
boolean
Alias
- UMLS CUI [1]
- C0018802
Description
If yes, specify grade at study start
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0018802
- UMLS CUI [1,2]
- C0150312
- UMLS CUI [1,3]
- C2348558
Description
Congestive Heart Failure NYHA Classification
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0018802
- UMLS CUI [1,2]
- C1275491
Description
Past medical or surgical history
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0489540
Description
Past medical or surgical history - Details
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0489540
- UMLS CUI-3
- C1522508
Description
Past medical or surgical history
Type de données
text
Alias
- UMLS CUI [1]
- C0262926
- UMLS CUI [2]
- C0489540
Description
Past medical or surgical history: persistent symptoms
Type de données
text
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C1457887
- UMLS CUI [1,3]
- C0205322
- UMLS CUI [2,1]
- C0489540
- UMLS CUI [2,2]
- C1457887
- UMLS CUI [2,3]
- C0205322
Similar models
Medical/Surgical History, VTE Risk Factors
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,2])
C0035648 (UMLS CUI-2)
C1861172 (UMLS CUI-3)
C0679637 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0262926 (UMLS CUI [2,1])
C0332677 (UMLS CUI [2,2])
C0332185 (UMLS CUI [2,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C0150312 (UMLS CUI [1,2])
C2348558 (UMLS CUI [1,3])
C1275491 (UMLS CUI [1,2])
C0489540 (UMLS CUI-2)
C0262926 (UMLS CUI [1,2])
C0205394 (UMLS CUI [2,1])
C0489540 (UMLS CUI [2,2])
C0489540 (UMLS CUI-2)
C1522508 (UMLS CUI-3)
C0489540 (UMLS CUI [2])
C1457887 (UMLS CUI [1,2])
C0205322 (UMLS CUI [1,3])
C0489540 (UMLS CUI [2,1])
C1457887 (UMLS CUI [2,2])
C0205322 (UMLS CUI [2,3])