ID
37703
Description
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
Keywords
Versions (1)
- 8/19/19 8/19/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
August 19, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Oral Topotecan as Radiosensitizing Agent in Patients with Rectal Cancer; NCT00158886
Concomitant Medication
- StudyEvent: ODM
Description
Concomitant Medication
Alias
- UMLS CUI-1
- C2347852
Description
Concomitant Agent, Medication name
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Description
Concomitant Agent, Unit of Measure, Dosage
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C1519795
- UMLS CUI [1,3]
- C0178602
Description
Concomitant Agent, Frequencies
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439603
Description
Concomitant Agent, Drug Administration Routes
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0013153
Description
Concomitant Agent, Disease
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0012634
Description
Concomitant Medication Start Date
Data type
date
Alias
- UMLS CUI [1]
- C2826734
Description
Concomitant Medication End Date
Data type
date
Alias
- UMLS CUI [1]
- C2826744
Description
Concomitant Medication Ongoing
Data type
boolean
Alias
- UMLS CUI [1]
- C2826666
Similar models
Concomitant Medication
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0439603 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])