ID

9194

Descrizione

CALGB: 10201 Treatment FORM Daunorubicin and Cytarabine With or Without Oblimersen in Treating Older Patients With Previously Untreated Acute Myeloid Leukemia Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=AD83D624-B33F-3003-E034-0003BA12F5E7

collegamento

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=AD83D624-B33F-3003-E034-0003BA12F5E7

Keywords

  1. 19/09/12 19/09/12 -
  2. 09/01/15 09/01/15 - Martin Dugas
Caricato su

9 gennaio 2015

DOI

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Licenza

Creative Commons BY-NC 3.0 Legacy

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Leukemia NCT00085124 Treatment - CALGB: 10201 Treatment FORM - 2031608v3.0

Instructions: Complete and submit thie form as required by the protocol. Information in the upper right box must be completed for this form to be accepted. For optimal accuracy use black ink. Mark an X in the appropriate box for fields with a choice. Print text in capital letters. Avoid contact with the edges of the boxes. Cirlce amended items and check "Amended data" box to teh right. If submitting by mail, retain a copy for your records and send the original form for mazimum clarity in transmission and fax to 919-416-4990. If submistting electronically, click the Send button when you have completed the PDF version of the form.

Calgb Form
Descrizione

Calgb Form

CALGB Study No.
Descrizione

CALGBProtocolNumber

Tipo di dati

text

CALGB Patient ID
Descrizione

CALGBPatientID

Tipo di dati

text

Are data amended?
Descrizione

AmendedDataInd

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C25474
UMLS 2011AA ObjectClass
C1511726
NCI Thesaurus Property
C25416
UMLS 2011AA Property
C1691222
Patient's Initials (Last, First, Middle)
Descrizione

Patient Initials

Tipo di dati

text

Alias
NCI Thesaurus ValueDomain
C25191
UMLS CUI-1
C2986440
NCI Thesaurus ObjectClass
C16960
NCI Thesaurus Property
C25536
Participating Group
Descrizione

ParticipatingGroup

Tipo di dati

text

Alias
NCI Thesaurus ObjectClass
C17005
UMLS 2011AA ObjectClass
C1257890
NCI Thesaurus Property
C25364
UMLS 2011AA Property
C0600091
Patient Hospital No.
Descrizione

PatientHospitalNumber

Tipo di dati

text

Participating Group Protocol No.
Descrizione

ParticipatingGroupProtocolNo.

Tipo di dati

text

Institution/Affiliate
Descrizione

MainMemberInstitution/Affiliate

Tipo di dati

text

Participating Group Patient ID:
Descrizione

ParticipatingGroupPatientID

Tipo di dati

text

Reporting period Start Date
Descrizione

IntervalReportFromDate

Tipo di dati

date

Reporting period Start Date
Descrizione

IntervalReportFromDate

Tipo di dati

date

Reporting period End Date (MM DD YYYY)
Descrizione

IntervalReportToDate

Tipo di dati

date

Reporting period End Date (MM DD YYYY)
Descrizione

IntervalReportToDate

Tipo di dati

date

Treatment Phase Information
Descrizione

Treatment Phase Information

Treatment Phase (Mark one with an X)
Descrizione

TreatmentPhase

Tipo di dati

text

Other, specify (treatment phase)
Descrizione

TreatmentPhase,Other

Tipo di dati

text

Leukemia Treatment Plan
Descrizione

Leukemia Treatment Plan

Did the patient receive any protocol treatment?
Descrizione

ProtocolTreatmentInd

Tipo di dati

boolean

Date of first dose for this reporting period (MM DD YYYY)
Descrizione

TreatmentFirstDoseBeginDate

Tipo di dati

date

Number of courses or cycles given this reporting period
Descrizione

TotalCourseNumber

Tipo di dati

float

Date of last dose for this reporting period (MM DD YYYY)
Descrizione

TreatmentLastDoseEndDate

Tipo di dati

date

G3139 (dose) (mg)
Descrizione

AgentTotalDose

Tipo di dati

float

G3139 (dose) (mg)
Descrizione

AgentTotalDose

Tipo di dati

float

G3139 (dose) (mg)
Descrizione

AgentTotalDose

Tipo di dati

float

If the treatment ended this period, reason treatment ended or not given (Mark one with an X)
Descrizione

OffTreatmentReason

Tipo di dati

text

Other, specify (reason treatment ended)
Descrizione

OffTreatmentReason,Other

Tipo di dati

text

Were there any dose modifications or additions/omissions to protocol treatment (Mark one with an X)
Descrizione

DoseModification(Change)

Tipo di dati

text

If yes, unplanned, specify change
Descrizione

DoseModificationReason

Tipo di dati

text

Completed by (First Name, Last Name)
Descrizione

CompletedBy

Tipo di dati

text

Ccrr Module For Calgb: 10201 Treatment Form
Descrizione

Ccrr Module For Calgb: 10201 Treatment Form

Similar models

Instructions: Complete and submit thie form as required by the protocol. Information in the upper right box must be completed for this form to be accepted. For optimal accuracy use black ink. Mark an X in the appropriate box for fields with a choice. Print text in capital letters. Avoid contact with the edges of the boxes. Cirlce amended items and check "Amended data" box to teh right. If submitting by mail, retain a copy for your records and send the original form for mazimum clarity in transmission and fax to 919-416-4990. If submistting electronically, click the Send button when you have completed the PDF version of the form.

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Calgb Form
CALGBProtocolNumber
Item
CALGB Study No.
text
CALGBPatientID
Item
CALGB Patient ID
text
AmendedDataInd
Item
Are data amended?
text
C25474 (NCI Thesaurus ObjectClass)
C1511726 (UMLS 2011AA ObjectClass)
C25416 (NCI Thesaurus Property)
C1691222 (UMLS 2011AA Property)
Patient Initials
Item
Patient's Initials (Last, First, Middle)
text
C25191 (NCI Thesaurus ValueDomain)
C2986440 (UMLS CUI-1)
C16960 (NCI Thesaurus ObjectClass)
C25536 (NCI Thesaurus Property)
ParticipatingGroup
Item
Participating Group
text
C17005 (NCI Thesaurus ObjectClass)
C1257890 (UMLS 2011AA ObjectClass)
C25364 (NCI Thesaurus Property)
C0600091 (UMLS 2011AA Property)
PatientHospitalNumber
Item
Patient Hospital No.
text
ParticipatingGroupProtocolNo.
Item
Participating Group Protocol No.
text
MainMemberInstitution/Affiliate
Item
Institution/Affiliate
text
ParticipatingGroupPatientID
Item
Participating Group Patient ID:
text
IntervalReportFromDate
Item
Reporting period Start Date
date
IntervalReportFromDate
Item
Reporting period Start Date
date
IntervalReportToDate
Item
Reporting period End Date (MM DD YYYY)
date
IntervalReportToDate
Item
Reporting period End Date (MM DD YYYY)
date
Item Group
Treatment Phase Information
Item
Treatment Phase (Mark one with an X)
text
Code List
Treatment Phase (Mark one with an X)
CL Item
Current Phase Of Leukemia Treatment For Patient Is Induction (Induction)
CL Item
Current Phase Of Leukemia Treatment For Patient Is Consolidation (Consolidation)
CL Item
Current Phase Of Leukemia Treatment For Patient Is Follow-up, Or Patient Is Off Therapy (Follow-Up/Off Therapy)
CL Item
Current Phase Of Leukemia Treatment For Patient Is Specified Other Phase (Other, specify)
TreatmentPhase,Other
Item
Other, specify (treatment phase)
text
Item Group
Leukemia Treatment Plan
ProtocolTreatmentInd
Item
Did the patient receive any protocol treatment?
boolean
TreatmentFirstDoseBeginDate
Item
Date of first dose for this reporting period (MM DD YYYY)
date
TotalCourseNumber
Item
Number of courses or cycles given this reporting period
float
TreatmentLastDoseEndDate
Item
Date of last dose for this reporting period (MM DD YYYY)
date
AgentTotalDose
Item
G3139 (dose) (mg)
float
AgentTotalDose
Item
G3139 (dose) (mg)
float
AgentTotalDose
Item
G3139 (dose) (mg)
float
Item
If the treatment ended this period, reason treatment ended or not given (Mark one with an X)
text
Code List
If the treatment ended this period, reason treatment ended or not given (Mark one with an X)
CL Item
Treatment Completed Per Protocol Criteria (Treatment completed per protocol criteria)
CL Item
Disease Progression, Relapse During Active Treatment (Disease progression, relapse during active treatment)
CL Item
Progression Of Disease Occurred Prior To The Patient Beginning Protocol Therapy (Disease progression, relapse prior to beginning protocol therapy)
CL Item
Toxicity/side Effects/complications (Toxicity/side effects/complications)
CL Item
Patient Withdrawal Or Refusal After Beginning Protocol Therapy (Patient withdraw or refusal after beginning protocol therapy)
CL Item
Patient Withdrawal Or Refusal Prior To Beginning Protocol Therapy (Patient withdraw or refusal before beginning protocol therapy)
CL Item
Death Of Patient Occurred After The Patient Began Protocol Therapy (Death after beginning protocol therapy)
CL Item
Death Prior To Beginning Protocol Therapy (Death prior to beginning protocol therapy)
CL Item
Alternative Therapy (Alternative therapy)
CL Item
Other (Other complicating disease)
C17649 (NCI Thesaurus)
C0205394 (UMLS 2011AA)
CL Item
Other, Specify (Other, specify)
OffTreatmentReason,Other
Item
Other, specify (reason treatment ended)
text
Item
Were there any dose modifications or additions/omissions to protocol treatment (Mark one with an X)
text
Code List
Were there any dose modifications or additions/omissions to protocol treatment (Mark one with an X)
CL Item
No (No)
C49487 (NCI Thesaurus)
C1298908 (UMLS 2011AA)
CL Item
(i.e., The Treatment Was Changed According To Protocol Guidelines) (Yes, planned)
CL Item
(i.e., The Treatment Change Was Not Part Of Protocol Guidelines) (Yes, unplanned)
DoseModificationReason
Item
If yes, unplanned, specify change
text
CompletedBy
Item
Completed by (First Name, Last Name)
text
Item Group
Ccrr Module For Calgb: 10201 Treatment Form

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