ID
35355
Beschreibung
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma
Stichworte
Versionen (3)
- 01.03.19 01.03.19 -
- 01.03.19 01.03.19 -
- 30.10.19 30.10.19 - Sarah Riepenhausen
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
1. März 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556
Cycle 2 Day - Vital Signs; SRT501 Administration; Study Treatment Compliance (Issue); New Adverse Events and Concomitant Treatment
Beschreibung
Visit Date
Alias
- UMLS CUI-1
- C1320303
Beschreibung
Vital Signs
Alias
- UMLS CUI-1
- C0518766
Beschreibung
If Yes, complete below
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C1516048
Beschreibung
Date of assessment
Datentyp
date
Alias
- UMLS CUI [1]
- C2985720
Beschreibung
Check one box only
Datentyp
integer
Alias
- UMLS CUI [1]
- C1262869
Beschreibung
Systolic BP
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschreibung
Diastolic BP
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschreibung
Heart Rate
Datentyp
integer
Maßeinheiten
- beats/min
Alias
- UMLS CUI [1]
- C0018810
Beschreibung
Respiration Rate
Datentyp
integer
Maßeinheiten
- breaths/min
Alias
- UMLS CUI [1]
- C0231832
Beschreibung
Temperature
Datentyp
float
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
Check one box only
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0005903
- UMLS CUI [1,2]
- C1519795
Beschreibung
Weight
Datentyp
float
Alias
- UMLS CUI [1]
- C0005910
Beschreibung
Check one box only
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C0439148
Beschreibung
SRT501 Administration
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1320722
Beschreibung
Was SRT501 administered at this visit?
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1320722
Beschreibung
Date administered
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1521801
- UMLS CUI [1,2]
- C0011008
Beschreibung
Kit #
Datentyp
integer
Alias
- UMLS CUI [1]
- C2981406
Beschreibung
Time Administered
Datentyp
time
Alias
- UMLS CUI [1,1]
- C1521801
- UMLS CUI [1,2]
- C0040223
Beschreibung
Study Treatment Compliance (Issue)
Alias
- UMLS CUI-1
- C1321605
Beschreibung
Check one box only If No, please complete the comments page or the protocol deviations page.
Datentyp
integer
Alias
- UMLS CUI [1]
- C3890583
Beschreibung
Check one box only If No, please complete the comments page or the protocol deviations page.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2698559
Beschreibung
New Adverse Events and Concomitant Treatment
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2347852
Beschreibung
If Yes, please record details on Adverse Events page.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2347852
Beschreibung
If Yes, please record details on Concomitant Treatment page.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2347852
- UMLS CUI [2,1]
- C0678766
- UMLS CUI [2,2]
- C0205217
- UMLS CUI [3,1]
- C0678766
- UMLS CUI [3,2]
- C0205216
- UMLS CUI [4,1]
- C0439603
- UMLS CUI [4,2]
- C0205217
- UMLS CUI [5,1]
- C0439603
- UMLS CUI [5,2]
- C0205216
Ähnliche Modelle
Cycle 2 Day - Vital Signs; SRT501 Administration; Study Treatment Compliance (Issue); New Adverse Events and Concomitant Treatment
C1516048 (UMLS CUI [1,2])
C1320722 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C2698559 (UMLS CUI [1,2])
C2347852 (UMLS CUI-2)
C0678766 (UMLS CUI [2,1])
C0205217 (UMLS CUI [2,2])
C0678766 (UMLS CUI [3,1])
C0205216 (UMLS CUI [3,2])
C0439603 (UMLS CUI [4,1])
C0205217 (UMLS CUI [4,2])
C0439603 (UMLS CUI [5,1])
C0205216 (UMLS CUI [5,2])