ID
42082
Beschreibung
Study ID: 104512 Clinical Study ID: 104512 Study Title: Phase I, Dose-Escalation Study of Iodine-131 Anti-B1 Antibody for Patients With Previously Treated Non Hodgkin's Lymphoma With More Than 25% Bone Marrow Involvement Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00992758 Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Iodine-131 Anti-B1 Antibody Trade Name: Tositumomab Study Indication: Lymphoma, Non-Hodgkin
Stichworte
Versionen (2)
- 29.03.21 29.03.21 -
- 29.03.21 29.03.21 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
29. März 2021
DOI
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Lizenz
Creative Commons BY 4.0
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Iodine-131 Anti-B1 Antibody for Patients With Previously Treated Non Hodgkin's Lymphoma NCT00992758
Infection Summary; Concomitant Medications and Transfusions; Adverse Experiences
Beschreibung
Infection Summary
Alias
- UMLS CUI-1
- C0009450
- UMLS CUI-2
- C1706244
Beschreibung
If No, do not complete remainder of form. If Yes, complete remainder of form.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C0205281
- UMLS CUI [2]
- C0243026
- UMLS CUI [3]
- C0032285
- UMLS CUI [4,1]
- C2603343
- UMLS CUI [4,2]
- C0679823
Beschreibung
If no invasive infection, record date of visit
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C0205281
- UMLS CUI [2]
- C1320303
Beschreibung
If invasive infection, enter date of infection
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C0205281
- UMLS CUI [2]
- C0011008
Beschreibung
Type of Infection
Datentyp
integer
Alias
- UMLS CUI [1]
- C0457463
Beschreibung
Specify other type of infection
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0457463
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C2348235
Beschreibung
Method of confirmation
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0025663
Beschreibung
Specify other method of confirmation
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0750484
- UMLS CUI [1,2]
- C0025663
- UMLS CUI [2]
- C2348235
- UMLS CUI [3]
- C0205394
Beschreibung
If Yes, complete remaining culture information
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0430400
Beschreibung
Infection Summary - Culture information
Alias
- UMLS CUI-1
- C0009450
- UMLS CUI-2
- C1706244
- UMLS CUI-3
- C0430400
- UMLS CUI-4
- C1533716
Beschreibung
Source Code
Datentyp
integer
Alias
- UMLS CUI [1]
- C1710131
Beschreibung
Specify other source code
Datentyp
text
Alias
- UMLS CUI [1]
- C1710131
- UMLS CUI [2]
- C0205394
- UMLS CUI [3]
- C2348235
Beschreibung
Culture Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0430400
- UMLS CUI [1,2]
- C0011008
Beschreibung
Culture Result
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0430400
- UMLS CUI [1,2]
- C1274040
Beschreibung
If positive result, indicate organism code
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C1446409
- UMLS CUI [2,1]
- C0029235
- UMLS CUI [2,2]
- C0805701
Beschreibung
Specify other organism
Datentyp
text
Alias
- UMLS CUI [1]
- C0029235
- UMLS CUI [2]
- C0205394
- UMLS CUI [3]
- C2348235
Beschreibung
Infection Summary - Anti-infective
Alias
- UMLS CUI-1
- C0009450
- UMLS CUI-2
- C1706244
- UMLS CUI-3
- C0003204
Beschreibung
Infection Summary - Anti-infective
Alias
- UMLS CUI-1
- C0009450
- UMLS CUI-2
- C1706244
- UMLS CUI-3
- C0003204
Beschreibung
Anti-Infective
Datentyp
text
Alias
- UMLS CUI [1]
- C0003204
Beschreibung
IV or PO
Datentyp
integer
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
Empiric or therapeutic?
Datentyp
integer
Alias
- UMLS CUI [1]
- C1880496
- UMLS CUI [2]
- C0302350
Beschreibung
Anti-infective therapy start date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1141958
- UMLS CUI [1,2]
- C0808070
Beschreibung
Anti-infective therapy stop date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1141958
- UMLS CUI [1,2]
- C0806020
Beschreibung
Anti-infective therapy ongoing?
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1141958
- UMLS CUI [1,2]
- C0549178
Beschreibung
Concomitant Medications and Transfusions
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C1879316
Beschreibung
Drug or Blood Product
Datentyp
text
Alias
- UMLS CUI [1]
- C0013227
- UMLS CUI [2]
- C0456388
Beschreibung
Medication Dose
Datentyp
text
Alias
- UMLS CUI [1]
- C3174092
Beschreibung
Medication Unit
Datentyp
text
Alias
- UMLS CUI [1]
- C2826646
Beschreibung
Medication Route
Datentyp
text
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
Medication Frequency
Datentyp
text
Alias
- UMLS CUI [1]
- C3476109
Beschreibung
Medication Start Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2826734
Beschreibung
Medication Stop Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2826744
Beschreibung
Medication Continuing?
Datentyp
text
Alias
- UMLS CUI [1]
- C2826666
Beschreibung
Adverse Experiences
Alias
- UMLS CUI-1
- C0877248
Beschreibung
Adverse Experiences
Alias
- UMLS CUI-1
- C0877248
Beschreibung
Adverse Experience Number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0237753
Beschreibung
Adverse Experience
Datentyp
text
Alias
- UMLS CUI [1]
- C0877248
Beschreibung
Adverse Experience Grade
Datentyp
text
Alias
- UMLS CUI [1]
- C2985911
Beschreibung
SERIOUS: Fatal or immediately life-threatening, permanently disabling, requires or prolongs hospitalization, congenital anomaly,cancer,or overdose
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1519255
Beschreibung
Adverse Experience Onset Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2985916
Beschreibung
Adverse Experience Stop Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0806020
Beschreibung
Adverse Experience Ongoing
Datentyp
text
Alias
- UMLS CUI [1]
- C2826663
Beschreibung
Therapeutic Measures - Drug
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0013227
Beschreibung
Record all that apply
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0079809
- UMLS CUI [1,3]
- C0205394
Beschreibung
Specify other therapeutic measure
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0079809
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [2]
- C2348235
Beschreibung
Adverse Experience Outcome
Datentyp
integer
Alias
- UMLS CUI [1]
- C1705586
Beschreibung
Adverse Experience Relationship to Drug
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439849
Beschreibung
Adverse Experiences - Investigator Signature
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2346576
Ähnliche Modelle
Infection Summary; Concomitant Medications and Transfusions; Adverse Experiences
C0237753 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,2])
C1704732 (UMLS CUI [1,2])
C0205281 (UMLS CUI [1,2])
C0243026 (UMLS CUI [2])
C0032285 (UMLS CUI [3])
C2603343 (UMLS CUI [4,1])
C0679823 (UMLS CUI [4,2])
C0205281 (UMLS CUI [1,2])
C1320303 (UMLS CUI [2])
C0205281 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0025663 (UMLS CUI [1,2])
C0025663 (UMLS CUI [1,2])
C2348235 (UMLS CUI [2])
C0205394 (UMLS CUI [3])
C1706244 (UMLS CUI-2)
C0430400 (UMLS CUI-3)
C1533716 (UMLS CUI-4)
C0205394 (UMLS CUI [2])
C2348235 (UMLS CUI [3])
C0011008 (UMLS CUI [1,2])
C1446409 (UMLS CUI [1,2])
C0029235 (UMLS CUI [2,1])
C0805701 (UMLS CUI [2,2])
C0205394 (UMLS CUI [2])
C2348235 (UMLS CUI [3])
C1706244 (UMLS CUI-2)
C0003204 (UMLS CUI-3)
C1706244 (UMLS CUI-2)
C0003204 (UMLS CUI-3)
C0302350 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C1879316 (UMLS CUI-2)
C0456388 (UMLS CUI [2])
C0237753 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0079809 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0079809 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [2])
C0013227 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C2346576 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])