ID

41473

Descrição

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 Concomitant Medications (Non-Continuous Infusion) Form has to be filled in each time any change in medication (except for those administered as a continuous infusion) occurs during the Study. Please use one Instance of this Form per medication administered.

Link

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

Palavras-chave

Versões (1)
  1. 21/10/2020 21/10/2020 -
Titular dos direitos

GlaxoSmithKline

Transferido a

21 de outubro de 2020

DOI

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Licença

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

Inglês

Concomitant Medications (Non-Continuous Infusion)

1 Formulários  
Administrative Data
Descrição

Administrative Data

Alias
UMLS CUI-1
C1320722
Site #
Descrição

Study centre number

Tipo de dados

integer

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

patient ID

Tipo de dados

integer

Alias
UMLS CUI [1]
C2348585
Visit Date
Descrição

visit date

Tipo de dados

date

Alias
UMLS CUI [1]
C1320303
Investigator Name
Descrição

Investigator Name

Tipo de dados

text

Alias
UMLS CUI [1]
C2826892
Check if (additional) supplemental instance of this form was used.
Descrição

Check this box on all instances except for the last one.

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1706499
Instance Number
Descrição

Fill in the instance number, starting from 1. On all instances except for the last one, the preceding box has to be checked.

Tipo de dados

integer

Alias
UMLS CUI [1,1]
C1516308
UMLS CUI [1,2]
C2348184
Check if No Concomitant Medications were given:
Descrição

Check if No Concomitant Medications were given:

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C1705847
UMLS CUI-3
C1511497
UMLS CUI-4
C0549184
Check if No Concomitant Medications were given:
Descrição

(except for continuous IV infusions) Otherwise, please complete below and do not record more than ONE medication on same instance. Include all medications taken within 14 days, and all investigational drugs taken within 30 days (if investigational drug is administered within 30 days, please contact Medical Monitor [protocol violation]), prior to initiation of Argatroban infusion, and throughout study and 30-day follow-up period.

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C1705847
UMLS CUI [1,3]
C1511497
UMLS CUI [1,4]
C0549184
Concomintant Medications (Non-Continuous Infusion)
Descrição

Concomintant Medications (Non-Continuous Infusion)

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C1705847
UMLS CUI-3
C1511497
Line #
Descrição

Use a new instance if more than 6 lines are required. Also do not record more than ONE medication on the same instance.

Tipo de dados

integer

Alias
UMLS CUI [1]
C2348184
Drug Name
Descrição

(Prefer Trade Name)

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2360065
UMLS CUI [1,2]
C2347852
Dose (Include Units)
Descrição

Concomitant agent dose and dose unit

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C3174092
UMLS CUI [2]
C2826646
Route
Descrição

Concomitant agent route of admission

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0013153
Route - specify:
Descrição

Concomitant agent route of admission - specify

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0013153
UMLS CUI [1,3]
C1521902
Frequency
Descrição

Concomitant agent dosing frequency

Tipo de dados

text

Alias
UMLS CUI [1]
C2826654
Start Date
Descrição

(dd-mmm-yyyy)

Tipo de dados

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0808070
Start Time
Descrição

(0000-2359)

Tipo de dados

time

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C1301880
Stop Date
Descrição

(dd-mmm-yyyy)

Tipo de dados

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0806020
Stop Time
Descrição

(0000-2359)

Tipo de dados

time

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C1522314
Check if Ongoing
Descrição

Concomitant agent ongoing

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2826666
Indication
Descrição

Concomitant agent indication

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C3146298
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Similar models

Concomitant Medications (Non-Continuous Infusion)

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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])
Additional form
Item
Check if (additional) supplemental instance of this form was used.
boolean
C1706499 (UMLS CUI [1])
CRF Sequential Number
Item
Instance Number
integer
C1516308 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Item Group
Check if No Concomitant Medications were given:
C2347852 (UMLS CUI-1)
C1705847 (UMLS CUI-2)
C1511497 (UMLS CUI-3)
C0549184 (UMLS CUI-4)
No concomitant medications
Item
Check if No Concomitant Medications were given:
boolean
C2347852 (UMLS CUI [1,1])
C1705847 (UMLS CUI [1,2])
C1511497 (UMLS CUI [1,3])
C0549184 (UMLS CUI [1,4])
Item Group
Concomintant Medications (Non-Continuous Infusion)
C2347852 (UMLS CUI-1)
C1705847 (UMLS CUI-2)
C1511497 (UMLS CUI-3)
Sequence number
Item
Line #
integer
C2348184 (UMLS CUI [1])
Concomitant agent name
Item
Drug Name
text
C2360065 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Concomitant agent dose and dose unit
Item
Dose (Include Units)
text
C2347852 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
C2826646 (UMLS CUI [2])
Item
Route
text
C2347852 (UMLS CUI [1,1])
C0013153 (UMLS CUI [1,2])
Concomitant agent route of admission
Code List
Route
CL Item
oral  (1)
CL Item
intravenous (2)
CL Item
subcutaneous (3)
CL Item
topical (4)
CL Item
inhalation (5)
CL Item
transdermal (6)
CL Item
rectal (7)
CL Item
Other, specify (8)
Concomitant agent route of admission - specify
Item
Route - specify:
text
C2347852 (UMLS CUI [1,1])
C0013153 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
Concomitant agent dosing frequency
Item
Frequency
text
C2826654 (UMLS CUI [1])
Concomitant agent start date
Item
Start Date
date
C2347852 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Concomitant agent start time
Item
Start Time
time
C2347852 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Concomitant agent stop date
Item
Stop Date
date
C2347852 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Concomitant agent stop time
Item
Stop Time
time
C2347852 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Concomitant agent ongoing
Item
Check if Ongoing
boolean
C2826666 (UMLS CUI [1])
Concomitant agent indication
Item
Indication
text
C2347852 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
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