ID

6281

Description

GOG-0262: Cycle Dose Drug Form (D2R) Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=

Lien

https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=

Mots-clés

  1. 18/12/2014 18/12/2014 - Martin Dugas
  2. 22/08/2015 22/08/2015 - Martin Dugas
Téléchargé le

18 décembre 2014

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0 Legacy

Modèle Commentaires :

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GOG-0262: Cycle Dose Drug Form (D2R) - 2917656v1.0

No Instruction available.

  1. StudyEvent: SE.0000
    1. No Instruction available.
Header Module
Description

Header Module

Date form originally completed (m d y)
Description

FormOriginalCompleteDate

Type de données

date

Date form amended (m d y)
Description

FormAmendedCompleteDate

Type de données

date

Person amending form, last name
Description

ResponsiblePersonReportingChangeLastName

Type de données

text

Patient Initials (First, Middle, Last)
Description

PatientInitialsName

Type de données

text

Patient Study ID
Description

PatientGynecologicOncologyGroupIdentifierNumber

Type de données

text

Person Completing Form, Last Name
Description

ResponsiblePersonLastName

Type de données

text

Treatment Cycle And Modification
Description

Treatment Cycle And Modification

Current Cycle Number
Description

TreatmentCurrentCourseNumber

Type de données

double

Cycle Delayed?
Description

TreatmentDelayedCycleInd-3

Type de données

text

Number of days treatment cycle was delayed
Description

TreatmentDelayDayCount

Type de données

double

Cycle delayed reason
Description

TreatmentDelayedCycleReason

Type de données

text

Cycle start date (Day 1 m d y)
Description

TreatmentCourseBeginDate

Type de données

date

Agent name (Drug)
Description

AgentName

Type de données

text

Agent Dose level (e.g. mg/m^2)
Description

AgentDoseLevelValue

Type de données

text

Were there any dose modifications or additions/omissions to protocol treatment (1=Yes, planned; 2 =Yes, unplanned; 3=No)
Description

DoseModificationInd

Type de données

text

Total dose of agents/drugs for this cycle
Description

AgentCourseTotalDose

Type de données

double

Units (eg. mg, kg)
Description

AgentDoseUOM

Type de données

text

Patient weight (kg)
Description

PatientWeightMeasurement

Type de données

double

Unités de mesure
  • Kg
Kg
Body Surface Area (m^2)
Description

PersonBodySurfaceAreaValue

Type de données

double

Unités de mesure
  • m2
m2
Performance status (Zubrod)
Description

PerformanceStatusAssessmentEasternCooperativeOncologyGroupScale

Type de données

text

Pretreatment Hematology And Chemistry Values
Description

Pretreatment Hematology And Chemistry Values

Assessment Date (m d y)
Description

LesionAssessmentDate

Type de données

date

Hemoglobin
Description

LaboratoryProcedureHemoglobinResultSpecifiedValue

Type de données

double

Unités de mesure
  • g/dL
g/dL
Peripheral Hematocrit Count (1000/L)
Description

LaboratoryProcedureErythrocyteResultCount

Type de données

double

Peripheral WBC Count (mm3)
Description

LaboratoryProcedureLeukocyteResultSpecifiedValue

Type de données

double

Unités de mesure
  • 1000/uL
1000/uL
Peripheral Granulocytes Count (mm3)
Description

LaboratoryProcedureGranulocyteResultCount

Type de données

double

Unités de mesure
  • 1000/uL
1000/uL
Peripheral Platelet Count (mm3)
Description

LaboratoryProcedurePlateletResultSpecifiedValue

Type de données

double

Unités de mesure
  • 1000/uL
1000/uL
PT (sec)
Description

LaboratoryProcedureProthrombinTimeResultValue

Type de données

double

Unités de mesure
  • seconds
seconds
PTT (sec) (sec)
Description

LaboratoryProcedurePartialThromboplastinTimeResultValue

Type de données

double

BUN (mg/dl)
Description

LaboratoryProcedureBloodUreaNitrogenResultUnspecifiedValue

Type de données

double

Creatinine (mg/dl)
Description

LaboratoryProcedureCreatinineResultSpecifiedValue

Type de données

double

Unités de mesure
  • mg/dL
mg/dL
Creatinine Clearance (ml/min)
Description

LaboratoryProcedureCreatinineClearanceOutcomeValue

Type de données

double

SGOT
Description

LaboratoryProcedureSerumGlutamicOxaloaceticTransferaseResultUnspecifiedValue

Type de données

double

Bilirubin
Description

LaboratoryProcedureTotalBilirubinResultValue

Type de données

double

Unités de mesure
  • mg/dL
mg/dL
Alkaline Phosphatase
Description

LaboratoryProcedureAlkalinePhosphataseResultValue

Type de données

double

Result of CA125 (IU/ml)
Description

LaboratoryProcedureCA-125AntigenTumorMarkerResultValue

Type de données

double

International Normalization Ratio (INR)
Description

LaboratoryProcedureInternationalNormalizationRatioResultValue

Type de données

double

Other, specify test
Description

LaboratoryProcedureSecondOptionalPerformedSpecify

Type de données

text

Other specify value
Description

LaboratoryProcedurePerformedValue

Type de données

double

Comments
Description

Comments

COMMENTS
Description

ResearchCommentsText

Type de données

text

Similar models

No Instruction available.

  1. StudyEvent: SE.0000
    1. No Instruction available.
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Header Module
FormOriginalCompleteDate
Item
Date form originally completed (m d y)
date
FormAmendedCompleteDate
Item
Date form amended (m d y)
date
ResponsiblePersonReportingChangeLastName
Item
Person amending form, last name
text
PatientInitialsName
Item
Patient Initials (First, Middle, Last)
text
PatientGynecologicOncologyGroupIdentifierNumber
Item
Patient Study ID
text
ResponsiblePersonLastName
Item
Person Completing Form, Last Name
text
Item Group
Treatment Cycle And Modification
TreatmentCurrentCourseNumber
Item
Current Cycle Number
double
Item
Cycle Delayed?
text
Code List
Cycle Delayed?
CL Item
No (No)
CL Item
Yes (Yes)
TreatmentDelayDayCount
Item
Number of days treatment cycle was delayed
double
Item
Cycle delayed reason
text
Code List
Cycle delayed reason
CL Item
Non Protocol Illness (Non protocol illness)
CL Item
Patient Refusal (Patient refusal)
CL Item
Personal Reasons (Personal reasons)
CL Item
Protocol Related Ae (Protocol related AE)
CL Item
Scheduling (Scheduling)
TreatmentCourseBeginDate
Item
Cycle start date (Day 1 m d y)
date
AgentName
Item
Agent name (Drug)
text
AgentDoseLevelValue
Item
Agent Dose level (e.g. mg/m^2)
text
Item
Were there any dose modifications or additions/omissions to protocol treatment (1=Yes, planned; 2 =Yes, unplanned; 3=No)
text
Code List
Were there any dose modifications or additions/omissions to protocol treatment (1=Yes, planned; 2 =Yes, unplanned; 3=No)
CL Item
Yes, Planned (i.e., The Treatment Was Changed According To Protocol Guidelines) (Yes, planned)
CL Item
Yes, Unplanned (i.e., The Treatment Change Was Not Part Of Protocol Guidelines) (Yes, unplanned)
CL Item
No (No)
AgentCourseTotalDose
Item
Total dose of agents/drugs for this cycle
double
AgentDoseUOM
Item
Units (eg. mg, kg)
text
PatientWeightMeasurement
Item
Patient weight (kg)
double
PersonBodySurfaceAreaValue
Item
Body Surface Area (m^2)
double
Code List
Performance status (Zubrod)
CL Item
Fully Active, Able To Carry On All Pre-disease Performance Without Restriction. (0)
CL Item
Restricted In Physically Strenuous Activity But Ambulatory And Able To Carry Out Work Of A Light Or Sedentary Nature, E.g., Light Housework, Office Work. (1)
CL Item
Ambulatory And Capable Of All Selfcare But Unable To Carry Out Any Work Activities. Up And About More Than 50% Of Waking Hours. (2)
CL Item
Capable Of Only Limited Selfcare, Confined To Bed Or Chair More Than 50% Of Waking Hours. (3)
CL Item
Completely Disabled. Cannot Carry On Any Selfcare. Totally Confined To Bed Or Chair. (4)
Item Group
Pretreatment Hematology And Chemistry Values
LesionAssessmentDate
Item
Assessment Date (m d y)
date
LaboratoryProcedureHemoglobinResultSpecifiedValue
Item
Hemoglobin
double
LaboratoryProcedureErythrocyteResultCount
Item
Peripheral Hematocrit Count (1000/L)
double
LaboratoryProcedureLeukocyteResultSpecifiedValue
Item
Peripheral WBC Count (mm3)
double
LaboratoryProcedureGranulocyteResultCount
Item
Peripheral Granulocytes Count (mm3)
double
LaboratoryProcedurePlateletResultSpecifiedValue
Item
Peripheral Platelet Count (mm3)
double
LaboratoryProcedureProthrombinTimeResultValue
Item
PT (sec)
double
LaboratoryProcedurePartialThromboplastinTimeResultValue
Item
PTT (sec) (sec)
double
LaboratoryProcedureBloodUreaNitrogenResultUnspecifiedValue
Item
BUN (mg/dl)
double
LaboratoryProcedureCreatinineResultSpecifiedValue
Item
Creatinine (mg/dl)
double
LaboratoryProcedureCreatinineClearanceOutcomeValue
Item
Creatinine Clearance (ml/min)
double
LaboratoryProcedureSerumGlutamicOxaloaceticTransferaseResultUnspecifiedValue
Item
SGOT
double
LaboratoryProcedureTotalBilirubinResultValue
Item
Bilirubin
double
LaboratoryProcedureAlkalinePhosphataseResultValue
Item
Alkaline Phosphatase
double
LaboratoryProcedureCA-125AntigenTumorMarkerResultValue
Item
Result of CA125 (IU/ml)
double
LaboratoryProcedureInternationalNormalizationRatioResultValue
Item
International Normalization Ratio (INR)
double
LaboratoryProcedureSecondOptionalPerformedSpecify
Item
Other, specify test
text
LaboratoryProcedurePerformedValue
Item
Other specify value
double
Item Group
Comments
ResearchCommentsText
Item
COMMENTS
text

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