ID

37740

Beschrijving

Study ID: 104864/517 Clinical Study ID: 104864/517 Study Title: A Phase I Study of Oral Topotecan as a Radiosensitizing Agent in Patients With Rectal Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00158886 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Topotecan + Radiation therapy Trade Name: N/A Study Indication: Rectal Cancer, Carcinoma, Renal Cell

Trefwoorden

Versies (1)
  1. 21-08-19 21-08-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

21 augustus 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Oral Topotecan as Radiosensitizing Agent in Patients with Rectal Cancer; NCT00158886

Engels

Patient Log

1 Formulieren  
  1. StudyEvent: ODM
    1. Patient Log
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Center number
Beschrijving

Study Coordinating Center, Identification number

Datatype

integer

Alias
UMLS CUI [1,1]
C2825181
UMLS CUI [1,2]
C1300638
Patient Log
Beschrijving

Patient Log

Alias
UMLS CUI-1
C0030705
UMLS CUI-2
C2828389
Investigator
Beschrijving

Patients, Exclusion, Investigator Name

Datatype

text

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C2828389
UMLS CUI [1,3]
C2826892
Patient Initials
Beschrijving

Patients, Exclusion, Person Initials

Datatype

text

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C2828389
UMLS CUI [1,3]
C2986440
Interview Date
Beschrijving

Patients, Exclusion, patient interview, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C2828389
UMLS CUI [1,3]
C0683518
UMLS CUI [1,4]
C0011008
Reason for Exclusion
Beschrijving

Patients, Exclusion, Reason and justification

Datatype

text

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C2828389
UMLS CUI [1,3]
C0566251
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Similar models

Patient Log

1 Formulieren
  1. StudyEvent: ODM
    1. Patient Log
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Study Coordinating Center, Identification number
Item
Center number
integer
C2825181 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Item Group
Patient Log
C0030705 (UMLS CUI-1)
C2828389 (UMLS CUI-2)
Patients, Exclusion, Investigator Name
Item
Investigator
text
C0030705 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C2826892 (UMLS CUI [1,3])
Patients, Exclusion, Person Initials
Item
Patient Initials
text
C0030705 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,3])
Patients, Exclusion, patient interview, Date in time
Item
Interview Date
date
C0030705 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C0683518 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Patients, Exclusion, Reason and justification
Item
Reason for Exclusion
text
C0030705 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Terug naar het begin van de pagina 

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