ID
41337
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 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. See https://clinicaltrials.gov/ct2/show/NCT00039858 The Hematology Form has to be filled in twice: first, at the screening visit (within 96 hours before treatment initiation) and second, within 24 hours of final infusion completion or at the 30-day follow-up visit, whichever comes first.
Link
https://clinicaltrials.gov/ct2/show/NCT00039858
Trefwoorden
Versies (2)
- 31-08-20 31-08-20 -
- 02-09-20 02-09-20 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
31 augustus 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 4.0
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Safety and Efficacy of Argatroban in Pediatric Patients, NCT00039858
Hematology (pre-/post-treatment)
- StudyEvent: ODM
Beschrijving
Hematology
Alias
- UMLS CUI-1
- C0474523
Beschrijving
(dd-mmm-yyyy)
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0018941
Beschrijving
(0000-2359)
Datatype
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0018941
Beschrijving
Laboratory procedures not performed - hematology
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C0445106
- UMLS CUI [1,3]
- C0474523
Beschrijving
(Lab name must match name on lab normals.)
Datatype
text
Alias
- UMLS CUI [1,1]
- C3258037
- UMLS CUI [1,2]
- C0474523
Beschrijving
Copy of hematology report attached
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0684224
- UMLS CUI [1,2]
- C0474523
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0518015
Beschrijving
Hemoglobin measurement - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C2826293
Beschrijving
Hemoglobin measurement - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0518014
Beschrijving
Hematocrit measurement - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0518014
- UMLS CUI [1,2]
- C2826293
Beschrijving
Hematocrit measurement - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0518014
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0032181
Beschrijving
Platelet count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0032181
- UMLS CUI [1,2]
- C2826293
Beschrijving
Platelet count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0032181
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0014772
Beschrijving
RBC count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0014772
- UMLS CUI [1,2]
- C2826293
Beschrijving
RBC count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0014772
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0023508
Beschrijving
WBC count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C2826293
Beschrijving
WBC count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0200633
Beschrijving
Neutrophil Cell Count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0200633
- UMLS CUI [1,2]
- C2826293
Beschrijving
Neutrophil Cell Count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0200633
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0200635
Beschrijving
Lymphocyte Cell Count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0200635
- UMLS CUI [1,2]
- C2826293
Beschrijving
Lymphocyte Cell Count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0200635
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0750880
Beschrijving
Monocyte Cell Count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0750880
- UMLS CUI [1,2]
- C2826293
Beschrijving
Monocyte Cell Count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0750880
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0750879
Beschrijving
Eosinophil Cell Count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0750879
- UMLS CUI [1,2]
- C2826293
Beschrijving
Eosinophil Cell Count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0750879
- UMLS CUI [1,2]
- C0947611
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1]
- C0200641
Beschrijving
Basophil Cell Count - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0200641
- UMLS CUI [1,2]
- C2826293
Beschrijving
Basophil Cell Count - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0200641
- UMLS CUI [1,2]
- C0947611
Beschrijving
(specify test name)
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0474523
- UMLS CUI [1,3]
- C1521902
Beschrijving
(numeric value only)
Datatype
float
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0474523
Beschrijving
Other hematologic test - clinical significance
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0474523
- UMLS CUI [1,3]
- C2826293
Beschrijving
Other hematologic test - comment
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0474523
- UMLS CUI [1,3]
- C0947611
Similar models
Hematology (pre-/post-treatment)
- StudyEvent: ODM
C0018941 (UMLS CUI [1,2])
C0018941 (UMLS CUI [1,2])
C0445106 (UMLS CUI [1,2])
C0474523 (UMLS CUI [1,3])
C0474523 (UMLS CUI [1,2])
C0474523 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C0474523 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0474523 (UMLS CUI [1,2])
C0474523 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,3])
C0474523 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,3])