Informations:
Erreur:
ID
13518
Description
Pilot Clinical Trial of Pazopanib in Patients With Relapsed or Refractory Acute Myeloid Leukemia (AML) or at Initial Diagnosis When no Intensive Treatment is Possible (PAZOPANIB-AML) https://clinicaltrials.gov/ct2/show/NCT01361334 Principal Investigator: PD Dr. Torsten Kessler, University Hospital Muenster, Germany
Lien
https://clinicaltrials.gov/ct2/show/NCT01361334
Mots-clés
Versions (3)
- 14/08/2015 14/08/2015 - Martin Dugas
- 11/01/2016 11/01/2016 -
- 11/02/2016 11/02/2016 -
Téléchargé le
11 février 2016
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Clinical examination AML Pazopanib NCT01361334
Clinical examination AML Pazopanib NCT01361334
- StudyEvent: SE
Similar models
Clinical examination AML Pazopanib NCT01361334
- StudyEvent: SE
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Patient ID (derived)
Item
Patient ID (derived)
text
C2348585 (UMLS CUI [1])
Item
Visit info/Therapeutic regimen timepoint
text
C1276413 (UMLS CUI [1,1])
C2348792 (UMLS CUI [1,2])
C2348792 (UMLS CUI [1,2])
CL Item
Baseline (1)
CL Item
Tag 1 (2)
CL Item
Tag 2 (3)
CL Item
Tag 7 (4)
CL Item
Tag 10 (5)
CL Item
Tag 14 (6)
CL Item
Tag 28 (7)
CL Item
Monat 2 (8)
CL Item
Monat 3 (9)
CL Item
Monat 6 (10)
CL Item
Monat 9 (11)
CL Item
Monat 12 (12)
CL Item
Progression - Rezidiv (13)
CL Item
Follow Up - Blatt Nr. 1 (14)
CL Item
Follow Up - Blatt Nr. 2 (15)
CL Item
Follow Up - Blatt Nr. 3 (16)
CL Item
Follow Up - Blatt Nr. 4 (17)
CL Item
ja (1)
Visitendatum ab Visite 2
Item
Date of visit, from visit 2 on
date
C0008952 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Item
Date of visit, from visit 2 on - status
text
C0008952 (UMLS CUI [1])
CL Item
T (1)
CL Item
TM (2)
CL Item
M (3)
Item
Visit done: no, but Patient stays on study
text
C0008952 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,2])
CL Item
nein, Patient verbleibt aber in der Studie (0)
Item
Visit done: patient off study
text
C1518546 (UMLS CUI [1])
CL Item
study exit (9)
Klinischer Befund: Datum
Item
Clinical findings: date
date
C0582103 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Item
Clinical findings, status date
text
C0582103 (UMLS CUI [1,1])
C2985875 (UMLS CUI [1,2])
C2985875 (UMLS CUI [1,2])
CL Item
T (1)
CL Item
TM (2)
CL Item
M (3)
CL Item
ECOG-Status 0 (0)
C1828078 (UMLS CUI-1)
CL Item
ECOG-Status 1 (1)
C1827388 (UMLS CUI-1)
CL Item
ECOG-Status 2 (2)
C1828242 (UMLS CUI-1)
CL Item
ECOG-Status 3 (3)
C1827126 (UMLS CUI-1)
CL Item
ECOG-Status 4 (4)
C1827528 (UMLS CUI-1)
CL Item
nd (9)
Weight
Item
Weight
integer
C0005910 (UMLS CUI [1])
CL Item
nd (9)
Height
Item
Height
integer
C0005890 (UMLS CUI [1])
Pulse
Item
Pulse/Heart rate
integer
C0018810 (UMLS CUI [1])
CL Item
nd (9)
systolic
Item
Systolic blood pressure
integer
C0871470 (UMLS CUI [1])
diastolic
Item
Diastolic blood pressure
integer
C0428883 (UMLS CUI [1])
CL Item
nd (9)
QT interval
Item
QT interval
integer
C1287082 (UMLS CUI [1])
CL Item
nd (9)
CL Item
without pathological findings (1)
CL Item
pathologic findings, please specify (2)
Finding
Item
Finding
text
C0243095 (UMLS CUI [1])