ID

13575

Beschrijving

Phase 1 clinical trial for intrasurgical hyperthermic intraperitoneal chemoperfusion with cisplatin (HIPEC) in patients with ovarian cancer recidiv EudraCT Nr.: 2010-024352-28 Principal investigator und authorized representative of Sponsor: PD Dr. med. Oliver Zivanovic Center for Obstetrics and Gynaecology University Hospital Bonn Sigmund-Freud-Str. 25 53105 Bonn Sponsor: Rheinische Friedrich-Wilhelms-Universität Bonn represented by the Dean of Medical Faculty

Trefwoorden

Versies (2)
  1. 17-02-16 17-02-16 -
  2. 17-02-16 17-02-16 -
Geüploaded op

17 februari 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Adverse Events Phase 1 clinical trial for intrasurgical hyperthermic intraperitoneal chemoperfusion with cisplatin (HIPEC) in patients with ovarian cancer recidiv

Engels

Case Report Form (HIPEC) Adverse Events

1 Formulieren  
Adverse Events Form
Beschrijving

Adverse Events Form

Patient ID
Beschrijving

Patient ID

Datatype

integer

Alias
UMLS CUI [1]
C1269815
CRF number
Beschrijving

CRF number

Datatype

integer

Alias
UMLS CUI [1,1]
C1516308
UMLS CUI [1,2]
C0449788
Serial number of the Adverse Event
Beschrijving

Adverse Event

Datatype

integer

Alias
UMLS CUI [1]
C0877248
Please describe the Adverse Event, using CTCAE designations
Beschrijving

Adverse Event

Datatype

text

Alias
UMLS CUI [1]
C0877248
Adverse Event Start Date
Beschrijving

Adverse Event Start Date

Datatype

date

Alias
UMLS CUI [1]
C2697888
Adverse Event End Date
Beschrijving

Adverse Event End Date

Datatype

date

Alias
UMLS CUI [1]
C2697886
Is the Adverse Event Ongoing?
Beschrijving

Adverse Event Ongoing

Datatype

boolean

Alias
UMLS CUI [1]
C2826663
CTCAE Grade
Beschrijving

CTCAE Grade

Datatype

text

Alias
UMLS CUI [1]
C1516728
Was the Adverse Event serious (SAE)?
Beschrijving

Serious adverse event

Datatype

boolean

Alias
UMLS CUI [1]
C1519255
Criteria for serious adverse events, please specify
Beschrijving

Serious Adverse Event

Datatype

text

Alias
UMLS CUI [1]
C1519255
Please give the date, the adverse event turned out to be serious
Beschrijving

Serious adverse event start date

Datatype

date

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C0011008
Adverse Event Outcome
Beschrijving

Adverse Event Outcome

Datatype

text

Alias
UMLS CUI [1]
C1705586
Causality with trial substance
Beschrijving

Causality

Datatype

text

Alias
UMLS CUI [1]
C1547657
Adverse event treatment
Beschrijving

Adverse event treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0087111
Please specify treatment given for this adverse event
Beschrijving

Adverse event treatment

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0087111
Terug naar het begin van de pagina

Similar models

Case Report Form (HIPEC) Adverse Events

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Adverse Events Form
Patient ID
Item
Patient ID
integer
C1269815 (UMLS CUI [1])
CRF number
Item
CRF number
integer
C1516308 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Adverse Event
Item
Serial number of the Adverse Event
integer
C0877248 (UMLS CUI [1])
Adverse Event
Item
Please describe the Adverse Event, using CTCAE designations
text
C0877248 (UMLS CUI [1])
Adverse Event Start Date
Item
Adverse Event Start Date
date
C2697888 (UMLS CUI [1])
Adverse Event End Date
Item
Adverse Event End Date
date
C2697886 (UMLS CUI [1])
Adverse Event Ongoing
Item
Is the Adverse Event Ongoing?
boolean
C2826663 (UMLS CUI [1])
Item
CTCAE Grade
text
C1516728 (UMLS CUI [1])
CTCAE Grade
Code List
CTCAE Grade
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
0 (0)
Serious adverse event
Item
Was the Adverse Event serious (SAE)?
boolean
C1519255 (UMLS CUI [1])
Item
Criteria for serious adverse events, please specify
text
C1519255 (UMLS CUI [1])
Serious Adverse Event
Code List
Criteria for serious adverse events, please specify
CL Item
fatal (1)
CL Item
life threatening (2)
CL Item
hospitalization/prolonged stay at hospital (3)
CL Item
permanent or severe disability (4)
CL Item
congenital abberation/birth defect (5)
Serious adverse event start date
Item
Please give the date, the adverse event turned out to be serious
date
C1519255 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Adverse Event Outcome
text
C1705586 (UMLS CUI [1])
Adverse Event Outcome
Code List
Adverse Event Outcome
CL Item
Recovered (1)
CL Item
Subsiding (2)
CL Item
Continuing (3)
CL Item
resolved with sequelae (4)
CL Item
increased symptoms (5)
CL Item
fatal (6)
CL Item
unknown (7)
Item
Causality with trial substance
text
C1547657 (UMLS CUI [1])
Causality
Code List
Causality with trial substance
CL Item
confirmed (1)
CL Item
probable (2)
CL Item
possible (3)
CL Item
unlikely (4)
Adverse event treatment
Item
Adverse event treatment
boolean
C0877248 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Adverse event treatment
Item
Please specify treatment given for this adverse event
text
C0877248 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial