ID

41476

Beschrijving

Study ID: 105043/013 Clinical Study ID: 105043/013 Study Title: An Open-Label Study of Argatroban Injection to Evaluate the Safety and Effectiveness in Pediatric Patients Requiring Anticoagulant Alternatives to Heparin (Protocol SKF105043/013) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00039858 - See https://clinicaltrials.gov/ct2/show/NCT00039858 Sponsor: GlaxoSmithKline Collaborators: Encysive Pharmaceuticals Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Argatroban Trade Name: N/A Study Indication: Thrombosis This Study evaluates the safety and the efficacy of i.v. Argatroban treatment in paediatric patients which require anticoagulants but aren't suitable for Heparin treatment. The study consists of screening visit (pre-treatment examination), treatment period of maximum 14 days after reaching therapeutical dose, post-treatment visit (once the treatment is stopped or after 14 days) and a follow-up visit which follows 30 days (+/- 14 days) after clinical resolution of underlying condition or after the end of the 14-day study period. Treatment can be continued after the 14-day study period if needed but such treatment isn't part of this Study. The Clinical Endpoints Form has to be filled in on study conclusion. It is used to record if any of the mentioned Events happened during the Study.

Link

https://clinicaltrials.gov/ct2/show/NCT00039858

Trefwoorden

Versies (1)
  1. 21-10-20 21-10-20 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

21 oktober 2020

DOI

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Licentie

Creative Commons BY-NC 4.0
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Safety and Efficacy of Argatroban in Pediatric Patients, NCT00039858

Engels

Clinical Endpoints

1 Formulieren  
  1. StudyEvent: ODM
    1. Clinical Endpoints
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Site #
Beschrijving

Study centre number

Datatype

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Patient #
Beschrijving

patient ID

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Visit Date
Beschrijving

visit date

Datatype

date

Alias
UMLS CUI [1]
C1320303
Investigator Name
Beschrijving

Investigator Name

Datatype

text

Alias
UMLS CUI [1]
C2826892
Please mark all events that occurred during dosing:
Beschrijving

Please mark all events that occurred during dosing:

Alias
UMLS CUI-1
C2347784
(or None: please check this box)
Beschrijving

If None, check this Box and leave the following fields blank.

Datatype

boolean

Alias
UMLS CUI [1,1]
C2347784
UMLS CUI [1,2]
C0549184
Occurrence/Re-occurrence of thrombosis:
Beschrijving

Occurrence/Re-occurrence of thrombosis:

Alias
UMLS CUI-1
C2745955
UMLS CUI-2
C0040053
Venous thrombosis
Beschrijving

Venous thrombosis

Datatype

text

Alias
UMLS CUI [1]
C0042487
Venous thrombosis - specify location:
Beschrijving

Venous thrombosis - location

Datatype

text

Alias
UMLS CUI [1,1]
C0042487
UMLS CUI [1,2]
C0450429
Venous thrombosis - Date
Beschrijving

(dd-mmm-yyyy)

Datatype

date

Alias
UMLS CUI [1,1]
C0042487
UMLS CUI [1,2]
C0011008
Pulmonary embolus
Beschrijving

Pulmonary embolus

Datatype

text

Alias
UMLS CUI [1]
C0034065
Pulmonary embolus - Date
Beschrijving

(dd-mmm-yyyy)

Datatype

date

Alias
UMLS CUI [1,1]
C0034065
UMLS CUI [1,2]
C0011008
Arterial thrombosis
Beschrijving

Arterial thrombosis

Datatype

text

Alias
UMLS CUI [1]
C0151942
Arterial thrombosis - specify location:
Beschrijving

Arterial thrombosis - location

Datatype

text

Alias
UMLS CUI [1,1]
C0151942
UMLS CUI [1,2]
C0450429
Arterial thrombosis - Date
Beschrijving

(dd-mmm-yyyy)

Datatype

date

Alias
UMLS CUI [1,1]
C0151942
UMLS CUI [1,2]
C0011008
Clotting in any external circuit that requires immediate therapeutic intervention
Beschrijving

Clotting in external circuit that requires immediate intervention

Datatype

text

Alias
UMLS CUI [1]
C0949072
UMLS CUI [2,1]
C1708545
UMLS CUI [2,2]
C0205253
Clotting in any external circuit that requires immediate therapeutic intervention - specify circuit location:
Beschrijving

Clotting in external circuit that requires immediate intervention - specify circuit location

Datatype

text

Alias
UMLS CUI [1]
C0949072
UMLS CUI [2,1]
C1708545
UMLS CUI [2,2]
C0205253
UMLS CUI [3,1]
C2348235
UMLS CUI [3,2]
C0015354
Clotting in any external circuit that requires immediate therapeutic intervention - Date
Beschrijving

(dd-mmm-yyyy)

Datatype

date

Alias
UMLS CUI [1]
C0949072
UMLS CUI [2,1]
C1708545
UMLS CUI [2,2]
C0205253
UMLS CUI [3]
C0011008
Thromboembolic complications:
Beschrijving

Thromboembolic complications:

Alias
UMLS CUI-1
C0040038
UMLS CUI-2
C0009566
Death due to thromboembolic complication
Beschrijving

Death due to thromboembolic complication

Datatype

text

Alias
UMLS CUI [1,1]
C1705232
UMLS CUI [1,2]
C0040038
UMLS CUI [1,3]
C0009566
Death due to thromboembolic complication - Date
Beschrijving

(dd-mmm-yyyy)

Datatype

date

Alias
UMLS CUI [1,1]
C1705232
UMLS CUI [1,2]
C0040038
UMLS CUI [1,3]
C0009566
UMLS CUI [1,4]
C1148348
Amputation due to thromboembolic complication
Beschrijving

Amputation due to thromboembolic complication

Datatype

text

Alias
UMLS CUI [1,1]
C0002688
UMLS CUI [1,2]
C0040038
UMLS CUI [1,3]
C0009566
Amputation due to thromboembolic complication - Date
Beschrijving

(dd-mmm-yyyy)

Datatype

date

Alias
UMLS CUI [1,1]
C0002688
UMLS CUI [1,2]
C0040038
UMLS CUI [1,3]
C0009566
UMLS CUI [1,4]
C0011008
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Similar models

Clinical Endpoints

1 Formulieren
  1. StudyEvent: ODM
    1. Clinical Endpoints
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Study centre number
Item
Site #
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
patient ID
Item
Patient #
integer
C2348585 (UMLS CUI [1])
visit date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Investigator Name
Item
Investigator Name
text
C2826892 (UMLS CUI [1])
Item Group
Please mark all events that occurred during dosing:
C2347784 (UMLS CUI-1)
No clinical endpoints met
Item
(or None: please check this box)
boolean
C2347784 (UMLS CUI [1,1])
C0549184 (UMLS CUI [1,2])
Item Group
Occurrence/Re-occurrence of thrombosis:
C2745955 (UMLS CUI-1)
C0040053 (UMLS CUI-2)
Item
Venous thrombosis
text
C0042487 (UMLS CUI [1])
Venous thrombosis
Code List
Venous thrombosis
CL Item
Yes (Yes)
CL Item
No (No)
Venous thrombosis - location
Item
Venous thrombosis - specify location:
text
C0042487 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Venous thrombosis - date
Item
Venous thrombosis - Date
date
C0042487 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Pulmonary embolus
text
C0034065 (UMLS CUI [1])
Venous thrombosis
Code List
Pulmonary embolus
CL Item
Yes (Yes)
CL Item
No (No)
Pulmonary embolus - date
Item
Pulmonary embolus - Date
date
C0034065 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Arterial thrombosis
text
C0151942 (UMLS CUI [1])
Venous thrombosis
Code List
Arterial thrombosis
CL Item
Yes (Yes)
CL Item
No (No)
Arterial thrombosis - location
Item
Arterial thrombosis - specify location:
text
C0151942 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Arterial thrombosis - date
Item
Arterial thrombosis - Date
date
C0151942 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Clotting in any external circuit that requires immediate therapeutic intervention
text
C0949072 (UMLS CUI [1])
C1708545 (UMLS CUI [2,1])
C0205253 (UMLS CUI [2,2])
Venous thrombosis
Code List
Clotting in any external circuit that requires immediate therapeutic intervention
CL Item
Yes (Yes)
CL Item
No (No)
Clotting in external circuit that requires immediate intervention - specify circuit location
Item
Clotting in any external circuit that requires immediate therapeutic intervention - specify circuit location:
text
C0949072 (UMLS CUI [1])
C1708545 (UMLS CUI [2,1])
C0205253 (UMLS CUI [2,2])
C2348235 (UMLS CUI [3,1])
C0015354 (UMLS CUI [3,2])
Clotting in external circuit that requires immediate intervention - date
Item
Clotting in any external circuit that requires immediate therapeutic intervention - Date
date
C0949072 (UMLS CUI [1])
C1708545 (UMLS CUI [2,1])
C0205253 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3])
Item Group
Thromboembolic complications:
C0040038 (UMLS CUI-1)
C0009566 (UMLS CUI-2)
Item
Death due to thromboembolic complication
text
C1705232 (UMLS CUI [1,1])
C0040038 (UMLS CUI [1,2])
C0009566 (UMLS CUI [1,3])
Venous thrombosis
Code List
Death due to thromboembolic complication
CL Item
Yes (Yes)
CL Item
No (No)
Death due to thromboembolic complication - date
Item
Death due to thromboembolic complication - Date
date
C1705232 (UMLS CUI [1,1])
C0040038 (UMLS CUI [1,2])
C0009566 (UMLS CUI [1,3])
C1148348 (UMLS CUI [1,4])
Item
Amputation due to thromboembolic complication
text
C0002688 (UMLS CUI [1,1])
C0040038 (UMLS CUI [1,2])
C0009566 (UMLS CUI [1,3])
Venous thrombosis
Code List
Amputation due to thromboembolic complication
CL Item
Yes (Yes)
CL Item
No (No)
Amputation due to thromboembolic complication - date
Item
Amputation due to thromboembolic complication - Date
date
C0002688 (UMLS CUI [1,1])
C0040038 (UMLS CUI [1,2])
C0009566 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
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