ID
29858
Beschreibung
Study ID: 104864-201 Clinical Study ID: 104864/A201 Study Title: A Phase III, Open-Label, Multicenter, Randomized, Comparative Study of Topotecan, Ara-C and G-CSF (TAG) versus Idarubicin, Ara-C and G-CSF (IDAG) in MDS Patients with RAEB (High-Risk), RAEB-t or in Patients with AML from a Preceding Phase of MDS Patient Level Data: Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: topotecan Trade Name: hycamtin Study Indication: Myelodysplastic Syndrome https://www.gsk-clinicalstudyregister.com/study/104864/201?search=study&#rs
Link
https://www.gsk-clinicalstudyregister.com/study/104864/201?search=study&#rs
Stichworte
Versionen (1)
- 24.04.18 24.04.18 - Halim Ugurlu
Rechteinhaber
GSK
Hochgeladen am
24. April 2018
DOI
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Lizenz
Creative Commons BY-NC 3.0
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GSK Study ID 104864-201 Supportive Therapies-Transfusions, Anti-Infectives and Concominant Medication
Supportive Therapies-Transfusions, Anti-Infectives and Concominant Medication
Beschreibung
Supportive Therapy Transfusion
Alias
- UMLS CUI-1
- C1879316
- UMLS CUI-2
- C0014822
- UMLS CUI-3
- C0436313
Beschreibung
If Yes to Supportive Therapy (Including Erythropoietin)
Alias
- UMLS CUI-1
- C1879316
- UMLS CUI-2
- C0014822
- UMLS CUI-3
- C0436313
Beschreibung
Type of transfusions
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1879316
- UMLS CUI [1,2]
- C0332307
Beschreibung
Transfusions (Number of Units)
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1879316
- UMLS CUI [1,2]
- C0237753
Beschreibung
Erythropoietin Dose
Datentyp
float
Maßeinheiten
- units/kg
Alias
- UMLS CUI [1,1]
- C0014822
- UMLS CUI [1,2]
- C3174092
Beschreibung
Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1879316
Beschreibung
Supportive Anti-Infective Therapy
Alias
- UMLS CUI-1
- C1141958
- UMLS CUI-2
- C0436313
Beschreibung
If Yes to Supportive Anti-Infective Therapy
Alias
- UMLS CUI-1
- C1141958
- UMLS CUI-2
- C0436313
Beschreibung
If a treatment is recorded here, do not record on the Concomitant Medication section.
Datentyp
text
Alias
- UMLS CUI [1]
- C2360065
Beschreibung
Total Daily Dose
Datentyp
text
Alias
- UMLS CUI [1]
- C2348070
Beschreibung
For Route, see general instructions for acceptable abbreviations.
Datentyp
text
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
Where appropriate, medical conditions should be recorded in the Adverse Experiences section, utilizing the same terminology.
Datentyp
text
Alias
- UMLS CUI [1]
- C3843040
Beschreibung
Record PM for anti-infectives administered prophylactically, EM for anti-infectives used for symptomatic treatment, and TX for anti-infectives administered for a confirmed infection in the column provided.
Datentyp
text
Alias
- UMLS CUI [1]
- C1141958
Beschreibung
Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C3174092
Beschreibung
End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C3174092
Beschreibung
If Continuing to Medication
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0549178
Beschreibung
Concominant Medication
Alias
- UMLS CUI-1
- C2347852
Beschreibung
Record all concomitant medication taken during this course. Record PM for prophylactic treatment with Medical Condition for prophylactically administered medications. If a medication was marked 'Continuing' at the initial visit, it must be recorded below. Where appropriate, medical conditions should be recorded on the Adverse Experience Form, utilizing the same terminology
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C2347852
Beschreibung
Total Daily Dose
Datentyp
text
Alias
- UMLS CUI [1]
- C2348070
Beschreibung
For Route, see General Instructions for acceptable abbreviations
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0013153
- UMLS CUI [1,2]
- C2347852
Beschreibung
Medical Condition
Datentyp
text
Alias
- UMLS CUI [1]
- C3843040
Beschreibung
Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C2347852
Beschreibung
End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C2347852
Beschreibung
If Continung to Medication
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0549178
Ähnliche Modelle
Supportive Therapies-Transfusions, Anti-Infectives and Concominant Medication
C0014822 (UMLS CUI-2)
C0436313 (UMLS CUI-3)
C0014822 (UMLS CUI [1,2])
C0436313 (UMLS CUI [1,3])
C0014822 (UMLS CUI-2)
C0436313 (UMLS CUI-3)
C0332307 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C1879316 (UMLS CUI [1,2])
C0436313 (UMLS CUI-2)
C1514463 (UMLS CUI [1,2])
C1521721 (UMLS CUI [1,3])
C0436313 (UMLS CUI-2)
C3174092 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])