ID

38417

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 information on symptoms, diagnostics and treatment in case of a symptomatic DVT, and is to be filled in as appropriate during the study.

Lien

https://clinicaltrials.gov/ct2/show/NCT00038961

Mots-clés

Versions (1)
  1. 16/10/2019 16/10/2019 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

16 octobre 2019

DOI

Pour une demande vous connecter.

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

Anglais

Unscheduled Assessment of Symptomatic DVT

1 Formulaires  
Administrative data
Description

Administrative data

Alias
UMLS CUI-1
C1320722
Country No.
Description

Country No.

Type de données

integer

Alias
UMLS CUI [1,1]
C0454664
UMLS CUI [1,2]
C0600091
Centre No.
Description

Centre No.

Type de données

integer

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0600091
Subject No.
Description

Clinical Trial Subject Unique Identifier

Type de données

integer

Alias
UMLS CUI [1]
C2348585
Subject Initials
Description

Subject Initials

Type de données

text

Alias
UMLS CUI [1,1]
C1997894
UMLS CUI [1,2]
C2986440
General DVT Information
Description

General DVT Information

Alias
UMLS CUI-1
C1508263
UMLS CUI-2
C0149871
Date of first clinical signs/symptoms of DVT
Description

Date of first DVT signs/symptoms

Type de données

date

Alias
UMLS CUI [1,1]
C0149871
UMLS CUI [1,2]
C0574845
UMLS CUI [1,3]
C0037088
Side: Left
Description

DVT left side?

Type de données

boolean

Alias
UMLS CUI [1,1]
C0205091
UMLS CUI [1,2]
C0149871
UMLS CUI [1,3]
C0441987
Side: Right
Description

DVT right side?

Type de données

boolean

Alias
UMLS CUI [1,1]
C0149871
UMLS CUI [1,2]
C0441987
UMLS CUI [1,3]
C0205090
Ultrasonography
Description

Ultrasonography

Alias
UMLS CUI-1
C0041618
Not done
Description

If done, record date

Type de données

boolean

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C1272696
Date performed
Description

Ultrasonography date

Type de données

date

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C0011008
Ultrasonography Result of Left Common Femoral
Description

Ultrasonography Result of Left Common Femoral

Type de données

text

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C1275667
UMLS CUI [1,3]
C0205091
UMLS CUI [1,4]
C1274040
Ultrasonography Result of Left Popliteal
Description

Ultrasonography Result of Left Popliteal

Type de données

text

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C0032652
UMLS CUI [1,3]
C0205091
UMLS CUI [1,4]
C1274040
Ultrasonography Result of Right Common Femoral
Description

Ultrasonography Result of Right Common Femoral

Type de données

text

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C1275667
UMLS CUI [1,3]
C0205090
UMLS CUI [1,4]
C1274040
Ultrasonography Result of Right Popliteal
Description

Ultrasonography Result of Right Popliteal

Type de données

text

Alias
UMLS CUI [1,1]
C0041618
UMLS CUI [1,2]
C0032652
UMLS CUI [1,3]
C0205090
UMLS CUI [1,4]
C1274040
Venography
Description

Venography

Alias
UMLS CUI-1
C0031545
Venography Type
Description

For bilateral/left leg/right leg, record date in next item. For not done/left leg/right leg, record primary reason.

Type de données

text

Alias
UMLS CUI [1,1]
C0031545
UMLS CUI [1,2]
C0332307
Date performed
Description

Venography Date

Type de données

date

Alias
UMLS CUI [1,1]
C0031545
UMLS CUI [1,2]
C0011008
If NOT BILATERAL or NOT DONE, select the primary reason
Description

if other reason, specify in next item

Type de données

text

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C0031545
UMLS CUI [1,3]
C1272696
UMLS CUI [2,1]
C1549995
UMLS CUI [2,2]
C0205092
UMLS CUI [2,3]
C0031545
Specify other primary reason NOT BILATERAL or NOT DONE
Description

if applicable

Type de données

text

Alias
UMLS CUI [1,1]
C1521902
UMLS CUI [1,2]
C3840932
UMLS CUI [1,3]
C0031545
UMLS CUI [1,4]
C1272696
UMLS CUI [2,1]
C1521902
UMLS CUI [2,2]
C3840932
UMLS CUI [2,3]
C0205092
UMLS CUI [2,4]
C0031545
Treatment
Description

Treatment

Alias
UMLS CUI-1
C0087111
Based on signs and symptoms, ultrasound and/or venogram results, was medication given to treat DVT?
Description

If medication was given, record in the medication form

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0149871
UMLS CUI [1,3]
C0566251
UMLS CUI [1,4]
C0037088
UMLS CUI [2,1]
C0013216
UMLS CUI [2,2]
C0149871
UMLS CUI [2,3]
C0566251
UMLS CUI [2,4]
C0041618
UMLS CUI [3,1]
C0013216
UMLS CUI [3,2]
C0149871
UMLS CUI [3,3]
C0566251
UMLS CUI [3,4]
C0031545
Retour au début de la page

Similar models

Unscheduled Assessment of Symptomatic DVT

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Country No.
Item
Country No.
integer
C0454664 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Centre No.
Item
Centre No.
integer
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Clinical Trial Subject Unique Identifier
Item
Subject No.
integer
C2348585 (UMLS CUI [1])
Subject Initials
Item
Subject Initials
text
C1997894 (UMLS CUI [1,1])
C2986440 (UMLS CUI [1,2])
Item Group
General DVT Information
C1508263 (UMLS CUI-1)
C0149871 (UMLS CUI-2)
Date of first DVT signs/symptoms
Item
Date of first clinical signs/symptoms of DVT
date
C0149871 (UMLS CUI [1,1])
C0574845 (UMLS CUI [1,2])
C0037088 (UMLS CUI [1,3])
DVT left side?
Item
Side: Left
boolean
C0205091 (UMLS CUI [1,1])
C0149871 (UMLS CUI [1,2])
C0441987 (UMLS CUI [1,3])
DVT right side?
Item
Side: Right
boolean
C0149871 (UMLS CUI [1,1])
C0441987 (UMLS CUI [1,2])
C0205090 (UMLS CUI [1,3])
Item Group
Ultrasonography
C0041618 (UMLS CUI-1)
Ultrasonography not done
Item
Not done
boolean
C0041618 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Ultrasonography date
Item
Date performed
date
C0041618 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Ultrasonography Result of Left Common Femoral
text
C0041618 (UMLS CUI [1,1])
C1275667 (UMLS CUI [1,2])
C0205091 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Ultrasonography, Common Femoral vein, left, Result
Code List
Ultrasonography Result of Left Common Femoral
CL Item
Fully compressible/Normal (Fully compressible/Normal)
CL Item
Non compressible (Non compressible)
CL Item
Inadequate (Inadequate)
CL Item
Not done (Not done)
Item
Ultrasonography Result of Left Popliteal
text
C0041618 (UMLS CUI [1,1])
C0032652 (UMLS CUI [1,2])
C0205091 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Ultrasonography, Common Femoral vein, left, Result
Code List
Ultrasonography Result of Left Popliteal
CL Item
Fully compressible/Normal (Fully compressible/Normal)
CL Item
Non compressible (Non compressible)
CL Item
Inadequate (Inadequate)
CL Item
Not done (Not done)
Item
Ultrasonography Result of Right Common Femoral
text
C0041618 (UMLS CUI [1,1])
C1275667 (UMLS CUI [1,2])
C0205090 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Ultrasonography, Common Femoral vein, left, Result
Code List
Ultrasonography Result of Right Common Femoral
CL Item
Fully compressible/Normal (Fully compressible/Normal)
CL Item
Non compressible (Non compressible)
CL Item
Inadequate (Inadequate)
CL Item
Not done (Not done)
Item
Ultrasonography Result of Right Popliteal
text
C0041618 (UMLS CUI [1,1])
C0032652 (UMLS CUI [1,2])
C0205090 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,4])
Ultrasonography, Common Femoral vein, left, Result
Code List
Ultrasonography Result of Right Popliteal
CL Item
Fully compressible/Normal (Fully compressible/Normal)
CL Item
Non compressible (Non compressible)
CL Item
Inadequate (Inadequate)
CL Item
Not done (Not done)
Item Group
Venography
C0031545 (UMLS CUI-1)
Item
Venography Type
text
C0031545 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Venography Type
Code List
Venography Type
CL Item
Not done (ND)
CL Item
Bilateral (BI)
CL Item
Left leg (L)
CL Item
Right leg (R)
Venography Date
Item
Date performed
date
C0031545 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
If NOT BILATERAL or NOT DONE, select the primary reason
text
C1549995 (UMLS CUI [1,1])
C0031545 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C1549995 (UMLS CUI [2,1])
C0205092 (UMLS CUI [2,2])
C0031545 (UMLS CUI [2,3])
Venography; Indication
Code List
If NOT BILATERAL or NOT DONE, select the primary reason
CL Item
Failed venous access (Failed venous access)
CL Item
Subject refused/withdrew consent (Subject refused/withdrew consent)
CL Item
Subject amputee (Subject amputee)
CL Item
Other, specify (Other, specify)
Specify other reason venography not done/unilateral
Item
Specify other primary reason NOT BILATERAL or NOT DONE
text
C1521902 (UMLS CUI [1,1])
C3840932 (UMLS CUI [1,2])
C0031545 (UMLS CUI [1,3])
C1272696 (UMLS CUI [1,4])
C1521902 (UMLS CUI [2,1])
C3840932 (UMLS CUI [2,2])
C0205092 (UMLS CUI [2,3])
C0031545 (UMLS CUI [2,4])
Item Group
Treatment
C0087111 (UMLS CUI-1)
Medication for DVT treatment given due to signs/symptoms/ultrasound/venography?
Item
Based on signs and symptoms, ultrasound and/or venogram results, was medication given to treat DVT?
boolean
C0013216 (UMLS CUI [1,1])
C0149871 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0037088 (UMLS CUI [1,4])
C0013216 (UMLS CUI [2,1])
C0149871 (UMLS CUI [2,2])
C0566251 (UMLS CUI [2,3])
C0041618 (UMLS CUI [2,4])
C0013216 (UMLS CUI [3,1])
C0149871 (UMLS CUI [3,2])
C0566251 (UMLS CUI [3,3])
C0031545 (UMLS CUI [3,4])
Retour au début de la page 

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