ID

31371

Beschrijving

Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Trefwoorden

  1. 22/07/2018 22/07/2018 -
  2. 18/08/2018 18/08/2018 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

18 de agosto de 2018

DOI

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Licentie

Creative Commons BY-NC 3.0

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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

Infection Summary (Visit 8)

Administrative
Beschrijving

Administrative

Alias
UMLS CUI-1
C1320722
Last Page
Beschrijving

Last Page

Datatype

boolean

Alias
UMLS CUI [1,1]
C1704732
UMLS CUI [1,2]
C1517741
Series page
Beschrijving

Series page

Datatype

text

Alias
UMLS CUI [1,1]
C0205549
UMLS CUI [1,2]
C1704732
Date of visit
Beschrijving

Date of visit

Datatype

date

Alias
UMLS CUI [1]
C1320303
Invasive infection
Beschrijving

Invasive infection

Alias
UMLS CUI-1
C0009450
UMLS CUI-2
C0205281
Has the patient had a presumed or confirmed invasive infection (e. g. sepsis, pneumonia, etc.) during study participation?
Beschrijving

Communicable Diseases; Invasive; Study; participation | Sepsis; Study; articipation | Pneumonia; Study; participation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205281
UMLS CUI [1,3]
C2603343
UMLS CUI [1,4]
C0679823
UMLS CUI [2,1]
C0243026
UMLS CUI [2,2]
C2603343
UMLS CUI [2,3]
C0679823
UMLS CUI [3,1]
C0032285
UMLS CUI [3,2]
C2603343
UMLS CUI [3,3]
C0679823
Type of infection (If the patient had an invasive infection, complete the rest of the form)
Beschrijving

Type of infection

Datatype

text

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0332307
If patient had other type of infection, please specify
Beschrijving

Communicable Diseases; Type - attribute; Other; Specification

Datatype

text

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C2348235
Method of confirmation
Beschrijving

Method of confirmation

Datatype

text

Alias
UMLS CUI [1,1]
C0750484
UMLS CUI [1,2]
C0025663
If other Method of confirmation, please specify
Beschrijving

Confirmation; Methods; Other; Specification

Datatype

text

Alias
UMLS CUI [1,1]
C0750484
UMLS CUI [1,2]
C0025663
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C2348235
Was a culture obtained?
Beschrijving

Blood culture

Datatype

boolean

Alias
UMLS CUI [1]
C0200949
Blood culture
Beschrijving

Blood culture

Alias
UMLS CUI-1
C0200949
Source Code
Beschrijving

Source Code

Datatype

text

Alias
UMLS CUI [1]
C1710131
If other Source Code, please specify
Beschrijving

Source Code; Other; Specification

Datatype

text

Alias
UMLS CUI [1,1]
C1710131
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C2348235
Sampling Date
Beschrijving

Sampling Date

Datatype

date

Alias
UMLS CUI [1,1]
C0870078
UMLS CUI [1,2]
C0011008
Sampling Result
Beschrijving

Sampling Result

Datatype

text

Alias
UMLS CUI [1,1]
C0870078
UMLS CUI [1,2]
C1274040
If positive, indicate organism code
Beschrijving

Result; Positive | Organism; Code

Datatype

text

Alias
UMLS CUI [1,1]
C1274040
UMLS CUI [1,2]
C1446409
UMLS CUI [2,1]
C0029235
UMLS CUI [2,2]
C0805701
If other organism code, please specify
Beschrijving

If other organism code, please specify

Datatype

text

Alias
UMLS CUI [1,1]
C0029235
UMLS CUI [1,2]
C0805701
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C2348235
Anti- infective
Beschrijving

Anti- infective

Alias
UMLS CUI-1
C0003204
Was an anti- infective administered?
Beschrijving

If yes, list here an on the Concomitant Medications form.

Datatype

boolean

Alias
UMLS CUI [1]
C0003204
Anti-Infectives
Beschrijving

Anti-Infectives

Alias
UMLS CUI-1
C0003204
Anti-Infective
Beschrijving

Anti-Infective Agents

Datatype

text

Alias
UMLS CUI [1]
C0003204
Empiric or therapeutic?
Beschrijving

Empiric | therapeutic

Datatype

text

Alias
UMLS CUI [1]
C1880496
UMLS CUI [2]
C0302350
Start date therapy
Beschrijving

Date treatment or therapy started

Datatype

date

Alias
UMLS CUI [1]
C3173309
Stop date therapy
Beschrijving

Date treatment stopped

Datatype

date

Alias
UMLS CUI [1]
C1531784
Therapy ongoing?
Beschrijving

Therapeutic procedure; Continuous

Datatype

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0549178

Similar models

Infection Summary (Visit 8)

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Last Page
Item
Last Page
boolean
C1704732 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
Series page
Item
Series page
text
C0205549 (UMLS CUI [1,1])
C1704732 (UMLS CUI [1,2])
Date of visit
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Item Group
Invasive infection
C0009450 (UMLS CUI-1)
C0205281 (UMLS CUI-2)
Communicable Diseases; Invasive; Study; participation | Sepsis; Study; articipation | Pneumonia; Study; participation
Item
Has the patient had a presumed or confirmed invasive infection (e. g. sepsis, pneumonia, etc.) during study participation?
boolean
C0009450 (UMLS CUI [1,1])
C0205281 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,3])
C0679823 (UMLS CUI [1,4])
C0243026 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
C0679823 (UMLS CUI [2,3])
C0032285 (UMLS CUI [3,1])
C2603343 (UMLS CUI [3,2])
C0679823 (UMLS CUI [3,3])
Item
Type of infection (If the patient had an invasive infection, complete the rest of the form)
text
C0009450 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Type of infection (If the patient had an invasive infection, complete the rest of the form)
CL Item
Meningitis (1)
CL Item
Pyelonephritis (2)
CL Item
Sepsis (3)
CL Item
Pneumonia (4)
CL Item
Endocarditis / Pericarditis (5)
CL Item
Peritonitis (6)
CL Item
Other (7)
Communicable Diseases; Type - attribute; Other; Specification
Item
If patient had other type of infection, please specify
text
C0009450 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Item
Method of confirmation
text
C0750484 (UMLS CUI [1,1])
C0025663 (UMLS CUI [1,2])
Code List
Method of confirmation
CL Item
PE (1)
CL Item
CT Scan (2)
CL Item
X-Ray (3)
CL Item
Other (4)
Confirmation; Methods; Other; Specification
Item
If other Method of confirmation, please specify
text
C0750484 (UMLS CUI [1,1])
C0025663 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Blood culture
Item
Was a culture obtained?
boolean
C0200949 (UMLS CUI [1])
Item Group
Blood culture
C0200949 (UMLS CUI-1)
Item
Source Code
text
C1710131 (UMLS CUI [1])
Code List
Source Code
CL Item
Sputum (1)
CL Item
Blood (2)
CL Item
Throat (3)
CL Item
Skin (4)
CL Item
CSF (5)
CL Item
Urine (6)
CL Item
Stool (7)
CL Item
Abscess (8)
CL Item
Other (9)
Source Code; Other; Specification
Item
If other Source Code, please specify
text
C1710131 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Sampling Date
Item
Sampling Date
date
C0870078 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Sampling Result
text
C0870078 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Code List
Sampling Result
CL Item
Positive (1)
CL Item
Negative (2)
Item
If positive, indicate organism code
text
C1274040 (UMLS CUI [1,1])
C1446409 (UMLS CUI [1,2])
C0029235 (UMLS CUI [2,1])
C0805701 (UMLS CUI [2,2])
Code List
If positive, indicate organism code
CL Item
Herpes simplex (1)
CL Item
Staph. aureus (2)
CL Item
Staph. epidermis (3)
CL Item
E. coli (4)
CL Item
Candida albicans (5)
CL Item
Strep. pneumoniae (6)
CL Item
Pseudomonas aeruginosa (7)
CL Item
Other (8)
If other organism code, please specify
Item
If other organism code, please specify
text
C0029235 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Item Group
Anti- infective
C0003204 (UMLS CUI-1)
Anti-Infective Agents
Item
Was an anti- infective administered?
boolean
C0003204 (UMLS CUI [1])
Item Group
Anti-Infectives
C0003204 (UMLS CUI-1)
Anti-Infective Agents
Item
Anti-Infective
text
C0003204 (UMLS CUI [1])
Item
Empiric or therapeutic?
text
C1880496 (UMLS CUI [1])
C0302350 (UMLS CUI [2])
Code List
Empiric or therapeutic?
CL Item
empiric (1)
CL Item
therapeutic (2)
Date treatment or therapy started
Item
Start date therapy
date
C3173309 (UMLS CUI [1])
Date treatment stopped
Item
Stop date therapy
date
C1531784 (UMLS CUI [1])
Item
Therapy ongoing?
text
C0087111 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
Code List
Therapy ongoing?
CL Item
yes (1)

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