ID
44476
Description
NCT00180102 AML2003 is a prospective randomized trial, to investigate the value of early allogeneic stem cell transplantation in aplasia after induction therapy for high risk patients with acute myeloid leukemia. Phase 4 Study Type:Interventional Study Design:Allocation: Randomized Intervention Model:Factorial Assignment Masking:None (Open Label) Primary Purpose:Treatment Medical Department I, University Hospital Carl Gustav Carus Dresden, Germany, 01307 Sponsors and Collaborators Technische Universität Dresden Principal Investigator:Gerhard Ehninger, MD University Hospital Carl Gustav Carus Dresden
Keywords
Versions (2)
- 1/19/18 1/19/18 -
- 9/27/21 9/27/21 -
Copyright Holder
Technische Universität Dresden,Dr. Röllig
Uploaded on
September 27, 2021
DOI
To request one please log in.
License
Creative Commons BY-NC 3.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
AML2003 - Standard-Therapy vs Intensified Therapy for Adult Acute Myeloid Leukemia Patients NCT00180102
Allogene SZT
- StudyEvent: ODM
- Eligibility criteria
- Ersterhebung
- Diagnostik vor Therapiebeginn
- 1. Induktionstherapie (DA)
- Induktionstherapie -Unerwünschte Ereignisse CTC 3.0-
- nach 1. Induktionstherapie
- 2. Induktionstherapie (DA)
- 2. Induktionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 2. Induktionstherapie
- 1. Postremissionstherapie (Ara-C/MAC)
- 1. Postremissionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 1. Postremissionstherapie
- 2. Postremissionstherapie (Ara-C/MAMAC)
- 2. Postremissionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 2. Postremissionstherapie
- 3. Postremissionstherapie (Ara-C/MAC)
- 3. Postremissionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 3. Postremissionstherapie
- Vor Stammzelltransplantation (SZT)
- Autologe SZT
- Allogene SZT
- SZT - Unerwünschte Ereignisse CTC 3.0 -
- Follow-up
- Rezidivbogen
- Schweres unerwünschtes Ereignis - SUE
Description
HLA-Kompatibilität
Alias
- UMLS CUI-1
- C0013018
- UMLS CUI-2
- C2348930
Description
Allogene SZT Konditionierung
Alias
- UMLS CUI-1
- C0376450
- UMLS CUI-2
- C1515895
Description
Conditioning agent Fludarabin
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0059985
- UMLS CUI [1,2]
- C0376450
Description
Treatment day fludarabine -6 bis -2
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0059985
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C0750480
Description
Fludarabine daily dose
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0059985
Description
Fludarabine cumulative dose
Data type
integer
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C2986497
- UMLS CUI [1,2]
- C0059985
Description
Conditioning agent Melphalan
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0025241
- UMLS CUI [1,2]
- C0376450
Description
Treatment day Melphalan
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0025241
- UMLS CUI [1,2]
- C0439228
- UMLS CUI [1,3]
- C0750480
Description
Melphalan daily dose
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0025241
Description
Melphalan cumulative dose
Data type
integer
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C2986497
- UMLS CUI [1,2]
- C0025241
Description
(wenn Fremdspender)
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0003442
- UMLS CUI [1,2]
- C0376450
Description
Treatment day ATG-Fresenius -5bis -2
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0439228
- UMLS CUI [1,2]
- C0750480
- UMLS CUI [1,3]
- C0003442
Description
ATG-Fresenius daily dose
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0003442
Description
ATG-Fresenius cumulative dose
Data type
integer
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C2986497
- UMLS CUI [1,2]
- C0003442
Description
Other Conditioning agent
Data type
text
Alias
- UMLS CUI [1,1]
- C0376450
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0013227
Description
Drug Administration Routes
Data type
text
Alias
- UMLS CUI [1]
- C0013153
Description
Treatment day
Data type
text
Alias
- UMLS CUI [1,1]
- C0439228
- UMLS CUI [1,2]
- C0750480
Description
Daily dose
Data type
text
Alias
- UMLS CUI [1]
- C2348070
Description
Cumulative dose
Data type
text
Alias
- UMLS CUI [1]
- C2986497
Description
Transplantat
Alias
- UMLS CUI-1
- C1504389
Description
Transplant type
Data type
integer
Alias
- UMLS CUI [1,1]
- C3840412
- UMLS CUI [1,2]
- C2242529
Description
nucleated cells
Data type
integer
Measurement units
- *10^8 /kg
Alias
- UMLS CUI [1,1]
- C1180059
- UMLS CUI [1,2]
- C0007584
Description
CD34+ Cells
Data type
integer
Measurement units
- *10^6/kg
Alias
- UMLS CUI [1]
- C1277788
Description
CD3 (T-Cells)
Data type
integer
Measurement units
- *10^5 /kg
Alias
- UMLS CUI [1]
- C2025558
Description
Complete Chimerism within 30 days
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0333678
- UMLS CUI [1,2]
- C3845590
Description
maximum value
Data type
integer
Measurement units
- %
Alias
- UMLS CUI [1,1]
- C0587081
- UMLS CUI [1,2]
- C0806909
Description
Date of complete chimerism
Data type
date
Alias
- UMLS CUI [1,1]
- C3703928
- UMLS CUI [1,2]
- C0011008
Description
Acute graft versus host disease
Data type
integer
Alias
- UMLS CUI [1]
- C0856825
Description
Gvhd grade skin
Data type
integer
Alias
- UMLS CUI [1,1]
- C4273340
- UMLS CUI [1,2]
- C0441800
Description
Gvhd grade colon
Data type
integer
Alias
- UMLS CUI [1,1]
- C1334228
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0009368
Description
Gvhd grade liver
Data type
integer
Alias
- UMLS CUI [1,1]
- C4273346
- UMLS CUI [1,2]
- C0441800
Description
Materialversand an Studienzentrale
Alias
- UMLS CUI-1
- C1524049
- UMLS CUI-2
- C0520510
Description
Bone marrow heparinized
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0019134
- UMLS CUI [1,2]
- C0005953
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
heparinized pB
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0019134
- UMLS CUI [1,2]
- C0229664
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
bone marrow smears
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0205451
- UMLS CUI [1,2]
- C1883469
- UMLS CUI [1,3]
- C2097112
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
peripheral blood smears
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0205451
- UMLS CUI [1,2]
- C1883469
- UMLS CUI [1,3]
- C2238079
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
Date of completion
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0850287
Description
Investigator name
Data type
text
Alias
- UMLS CUI [1]
- C2826892
Description
Investigator Signature
Data type
text
Alias
- UMLS CUI [1]
- C2346576
Description
Beurteilung Engraftment
Alias
- UMLS CUI-1
- C0301944
- UMLS CUI-2
- C1516048
Description
Engraftment
Data type
boolean
Alias
- UMLS CUI [1]
- C0301944
Description
3x >0,5 GPt/l bzw . ≥ 500 /μl
Data type
date
Alias
- UMLS CUI [1,1]
- C1882078
- UMLS CUI [1,2]
- C0011008
Description
Sustained
Data type
boolean
Alias
- UMLS CUI [1]
- C3827885
Description
3x >20 GPt/l bzw . ≥ 20.000 /μl
Data type
date
Alias
- UMLS CUI [1,1]
- C1882407
- UMLS CUI [1,2]
- C0011008
Description
Sustained
Data type
boolean
Alias
- UMLS CUI [1]
- C3827885
Description
3x >50 GPt/l bzw . ≥ 50.000 /μl
Data type
date
Alias
- UMLS CUI [1,1]
- C1882407
- UMLS CUI [1,2]
- C0011008
Description
Sustained
Data type
boolean
Alias
- UMLS CUI [1]
- C3827885
Description
Number red blood cell transfusions
Data type
integer
Alias
- UMLS CUI [1,1]
- C0086252
- UMLS CUI [1,2]
- C0750480
Description
sustained
Data type
boolean
Alias
- UMLS CUI [1]
- C0443318
Description
Platelet transfusion
Data type
integer
Alias
- UMLS CUI [1]
- C0086818
Description
Count of Platelet transfusions
Data type
integer
Alias
- UMLS CUI [1,1]
- C0086818
- UMLS CUI [1,2]
- C0750480
- UMLS CUI [1,3]
- C1277092
Description
Sustained
Data type
boolean
Alias
- UMLS CUI [1]
- C0443318
Description
Count of pooled platelet transfusions
Data type
integer
Alias
- UMLS CUI [1,1]
- C0086818
- UMLS CUI [1,2]
- C1277095
- UMLS CUI [1,3]
- C0750480
Description
Sustained
Data type
boolean
Alias
- UMLS CUI [1]
- C0443318
Description
Count of granulocyte transfusions
Data type
integer
Alias
- UMLS CUI [1,1]
- C0085430
- UMLS CUI [1,2]
- C0018183
- UMLS CUI [1,3]
- C0750480
Description
SCT specific adverse events
Data type
integer
Alias
- UMLS CUI [1,1]
- C0371849
- UMLS CUI [1,2]
- C0877248
Description
SCT specific adverse event , specify other
Data type
text
Alias
- UMLS CUI [1,1]
- C0371849
- UMLS CUI [1,2]
- C0877248
- UMLS CUI [1,3]
- C3845569
Description
Materialversand an Studienzentrale
Alias
- UMLS CUI-1
- C1524049
- UMLS CUI-2
- C0520510
Description
Bone marrow heparinized
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0019134
- UMLS CUI [1,2]
- C0005953
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
heparinized pB
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0019134
- UMLS CUI [1,2]
- C0229664
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
bone marrow smears
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0205451
- UMLS CUI [1,2]
- C1883469
- UMLS CUI [1,3]
- C2097112
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
peripheral blood smears
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0205451
- UMLS CUI [1,2]
- C1883469
- UMLS CUI [1,3]
- C2238079
Description
Shipping date
Data type
date
Alias
- UMLS CUI [1,1]
- C1524049
- UMLS CUI [1,2]
- C0011008
Description
KM-Morphologie
Alias
- UMLS CUI-1
- C2704380
Description
Bone marrow examination done?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0005957
- UMLS CUI [1,2]
- C0884358
Description
Date
Data type
date
Alias
- UMLS CUI [1]
- C0011008
Description
Not done reason
Data type
text
Alias
- UMLS CUI [1]
- C2826287
Description
Blasts in Bone marrow
Data type
integer
Measurement units
- %
Alias
- UMLS CUI [1]
- C1982687
Description
Laboratory Name
Data type
text
Alias
- UMLS CUI [1]
- C1882331
Description
Beurteilung des Therapieerfolges
Alias
- UMLS CUI-1
- C0085565
Description
Status post SCT
Data type
integer
Alias
- UMLS CUI [1,1]
- C0371849
- UMLS CUI [1,2]
- C0085415
Description
SCT associated death day number post-treatment
Data type
integer
Alias
- UMLS CUI [1,1]
- C0371849
- UMLS CUI [1,2]
- C0206277
- UMLS CUI [1,3]
- C2709088
Description
Date of completion
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0850287
Description
Investigator name
Data type
text
Alias
- UMLS CUI [1]
- C2826892
Description
Investigator Signature
Data type
text
Alias
- UMLS CUI [1]
- C2346576
Similar models
Allogene SZT
- StudyEvent: ODM
- Eligibility criteria
- Ersterhebung
- Diagnostik vor Therapiebeginn
- 1. Induktionstherapie (DA)
- Induktionstherapie -Unerwünschte Ereignisse CTC 3.0-
- nach 1. Induktionstherapie
- 2. Induktionstherapie (DA)
- 2. Induktionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 2. Induktionstherapie
- 1. Postremissionstherapie (Ara-C/MAC)
- 1. Postremissionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 1. Postremissionstherapie
- 2. Postremissionstherapie (Ara-C/MAMAC)
- 2. Postremissionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 2. Postremissionstherapie
- 3. Postremissionstherapie (Ara-C/MAC)
- 3. Postremissionstherapie - Unerwünschte Ereignisse CTC 3.0 -
- nach 3. Postremissionstherapie
- Vor Stammzelltransplantation (SZT)
- Autologe SZT
- Allogene SZT
- SZT - Unerwünschte Ereignisse CTC 3.0 -
- Follow-up
- Rezidivbogen
- Schweres unerwünschtes Ereignis - SUE
C2348930 (UMLS CUI [1,2])
(Comment:de)
(Comment:de)
(Comment:de)
C1515895 (UMLS CUI-2)
C0376450 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
C0059985 (UMLS CUI [1,2])
C0059985 (UMLS CUI [1,2])
C0376450 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
C0025241 (UMLS CUI [1,2])
C0025241 (UMLS CUI [1,2])
C0376450 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C0003442 (UMLS CUI [1,3])
C0003442 (UMLS CUI [1,2])
C0003442 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0750480 (UMLS CUI [1,2])
C2242529 (UMLS CUI [1,2])
C0007584 (UMLS CUI [1,2])
C3845590 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,2])
C0009368 (UMLS CUI [1,3])
C0520510 (UMLS CUI-2)
C0005953 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0229664 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1883469 (UMLS CUI [1,2])
C2097112 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C1883469 (UMLS CUI [1,2])
C2238079 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0850287 (UMLS CUI [1,2])
C1516048 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,2])
C1277092 (UMLS CUI [1,3])
C1277095 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
C0018183 (UMLS CUI [1,2])
C0750480 (UMLS CUI [1,3])
C0877248 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])
C3845569 (UMLS CUI [1,3])
C0520510 (UMLS CUI-2)
C0005953 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0229664 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1883469 (UMLS CUI [1,2])
C2097112 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C1883469 (UMLS CUI [1,2])
C2238079 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,2])
C0085415 (UMLS CUI [1,2])
C0206277 (UMLS CUI [1,2])
C2709088 (UMLS CUI [1,3])
C0850287 (UMLS CUI [1,2])