ID

37132

Description

Study ID: 104864/502 Clinical Study ID: 104864/502 Study Title: An Open-Label, Multicenter, Randomized, Phase II Study of Oral Topotecan Daily x 5 Days vs. Oral Topotecan 5 Days On, 2 Days Off for 3 Weeks for Second-Line Treatment in Patients with Recurrent, Locally Advanced or Metastatic Cervical Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan Trade Name: N/A Study Indication: Cancer, Locally Advanced or Metastatic Cervical Cancer

Keywords

Versions (1)
  1. 7/3/19 7/3/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 3, 2019

DOI

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License

Creative Commons BY-NC 3.0
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Oral Topotecan Daily x 5 Days vs. Oral Topotacan 5 Days On, 2 Days Off; 104864/502

English

Patient Log

1 forms  
  1. StudyEvent: ODM
    1. Patient Log
Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Center Number
Description

Institution name, Identifier

Data type

integer

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0600091
Patient Number
Description

Patient number

Data type

integer

Alias
UMLS CUI [1]
C1830427
Patient Initials
Description

Person Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Visit Date
Description

Date of visit

Data type

date

Alias
UMLS CUI [1]
C1320303
Patient Log
Description

Patient Log

Alias
UMLS CUI-1
C0030705
UMLS CUI-2
C1708728
Investigator
Description

Investigator Name

Data type

text

Alias
UMLS CUI [1]
C2826892
Patient Initials
Description

Person Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Interview Date
Description

Interview, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0021822
UMLS CUI [1,2]
C0011008
Reason for Exclusion
Description

Exclusion, Reason and Justification

Data type

text

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

Patient Log

1 forms
  1. StudyEvent: ODM
    1. Patient Log
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Institution name, Identifier
Item
Center Number
integer
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Patient number
Item
Patient Number
integer
C1830427 (UMLS CUI [1])
Person Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Date of visit
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Item Group
Patient Log
C0030705 (UMLS CUI-1)
C1708728 (UMLS CUI-2)
Investigator Name
Item
Investigator
text
C2826892 (UMLS CUI [1])
Person Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Interview, Date in time
Item
Interview Date
date
C0021822 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Exclusion, Reason and Justification
Item
Reason for Exclusion
text
C2828389 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
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