ID
37753
Beschreibung
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
Stichworte
Versionen (1)
- 21.08.19 21.08.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
21. August 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Oral Topotecan as Radiosensitizing Agent in Patients with Rectal Cancer; NCT00158886
Topotecan Post-Study Minimal Follow-up Report
- StudyEvent: ODM
Beschreibung
Month of Report
Alias
- UMLS CUI-1
- C1704685
- UMLS CUI-2
- C0439231
Beschreibung
Follow-Up Report, Month
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C0439231
Beschreibung
Follow-Up Report, Month
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C0439231
Beschreibung
Outcome
Alias
- UMLS CUI-1
- C1547647
Beschreibung
Patient Outcome, Cessation of life
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0011065
Beschreibung
Patient Outcome, Date last contact
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0805839
Beschreibung
Patient Outcome, Lost to follow-up
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C1302313
Beschreibung
Patient Outcome, Disease Progression
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0242656
Beschreibung
Patient Outcome, Disease Progression, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0242656
- UMLS CUI [1,3]
- C0011008
Beschreibung
Patient Outcome, Cancer treatment
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0920425
Beschreibung
Patient Outcome, Cancer treatment, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0920425
- UMLS CUI [1,3]
- C0808070
Beschreibung
Form D
Alias
- UMLS CUI-1
- C0011065
Beschreibung
Cause of Death
Datentyp
text
Alias
- UMLS CUI [1]
- C0007465
Beschreibung
Cause of Death
Datentyp
text
Alias
- UMLS CUI [1]
- C0007465
Beschreibung
Date of death
Datentyp
date
Alias
- UMLS CUI [1]
- C1148348
Beschreibung
Cessation of life, Autopsy
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0011065
- UMLS CUI [1,2]
- C0004398
Beschreibung
Cessation of life, Autopsy, Finding
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0011065
- UMLS CUI [1,2]
- C0004398
- UMLS CUI [1,3]
- C0243095
Beschreibung
Investigator's Signature
Alias
- UMLS CUI-1
- C2346576
Beschreibung
Investigator Signature
Datentyp
text
Alias
- UMLS CUI [1]
- C2346576
Beschreibung
Investigator Signature, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2346576
- UMLS CUI [1,2]
- C0011008
Ähnliche Modelle
Topotecan Post-Study Minimal Follow-up Report
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C0439231 (UMLS CUI [1,2])
C0439231 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C0805839 (UMLS CUI [1,2])
C1302313 (UMLS CUI [1,2])
C0242656 (UMLS CUI [1,2])
C0242656 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0920425 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0004398 (UMLS CUI [1,2])
C0004398 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])