ID

37272

Beschrijving

Study ID: 104864/902 Clinical Study ID: 104864/902 Study Title: An Open-Label, Single-Arm, Phase II Study of IV Weekly (Days 1 and 8 Every 21 Days) HYCAMTIN in Combination With Carboplatin (Day 1 Every 21 Days) as Second-Line Therapy in Subjects With Potentially Platinum-Sensitive Relapsed Ovarian Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00316173 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: topotecan Trade Name: CARBOPLATIN Study Indication: Ovarian Cancer; Neoplasms, Ovarian

Trefwoorden

Versies (1)
  1. 12-07-19 12-07-19 -
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GlaxoSmithKline

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12 juli 2019

DOI

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Creative Commons BY-NC 3.0
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HYCAMTIN in Combination With Carboplatin in Subjects with Ovarian Cancer; NCT00316173

Engels

End of Treatment

1 Formulieren  
  1. StudyEvent: ODM
    1. End of Treatment
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Beschrijving

Clinical Trial Subject Unique Identifier

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Vital Signs
Beschrijving

Vital Signs

Alias
UMLS CUI-1
C0518766
Weight
Beschrijving

Body Weight

Datatype

float

Maateenheden
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Blood pressure - Systolic
Beschrijving

Systolic Pressure

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
Blood pressure - Diastolic
Beschrijving

Diastolic blood pressure

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
Heart rate
Beschrijving

Heart rate

Datatype

integer

Maateenheden
  • bpm
Alias
UMLS CUI [1]
C0018810
bpm
Temperature
Beschrijving

Body Temperature

Datatype

float

Maateenheden
  • °C
Alias
UMLS CUI [1]
C0005903
°C
Lesion Assessment Using WHO Criteria - Indicator Lesions
Beschrijving

Lesion Assessment Using WHO Criteria - Indicator Lesions

Alias
UMLS CUI-1
C0221198
UMLS CUI-2
C1522602
UMLS CUI-3
C0220825
Lesion No.
Beschrijving

Lesion, Indicator, Numbers

Datatype

integer

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C0237753
Anatomic Description - Organ Code
Beschrijving

Lesion, Indicator, Organ, Code

Datatype

text

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C0178784
UMLS CUI [1,4]
C0805701
Anatomic Description - Lesion Location
Beschrijving

Lesion, Indicator, Location

Datatype

text

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C0450429
Date
Beschrijving

Lesion, Indicator, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C0011008
Can lesion be measured?
Beschrijving

Lesion, Indicator, Measurement method

Datatype

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C1299991
Diameter
Beschrijving

Lesion, Indicator, Diameter

Datatype

integer

Maateenheden
  • mm
Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C1301886
mm
Product
Beschrijving

Lesion, Indicator, Lesion size

Datatype

integer

Maateenheden
  • mm2
Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C0449453
mm2
Method
Beschrijving

Lesion, Indicator, Measurement method

Datatype

text

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C1299991
Lesion Code
Beschrijving

Lesion, Indicator, Lesion Code

Datatype

text

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1522602
UMLS CUI [1,3]
C0805701
Lesion Assessment Using WHO Criteria - Non-Measurable, Non-Evaluable Lesions
Beschrijving

Lesion Assessment Using WHO Criteria - Non-Measurable, Non-Evaluable Lesions

Alias
UMLS CUI-1
C1334988
UMLS CUI-2
C0220825
Lesion No.
Beschrijving

Non-Measurable Lesion, Numbers

Datatype

integer

Alias
UMLS CUI [1,1]
C1334988
UMLS CUI [1,2]
C0237753
Anatomic Description - Lesion Location
Beschrijving

Non-Measurable Lesion, Location

Datatype

text

Alias
UMLS CUI [1,1]
C1334988
UMLS CUI [1,2]
C0450429
Date
Beschrijving

Non-Measurable Lesion, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C1334988
UMLS CUI [1,2]
C0011008
Present
Beschrijving

Non-Measurable Lesion, Present

Datatype

text

Alias
UMLS CUI [1,1]
C1334988
UMLS CUI [1,2]
C0150312
Absent
Beschrijving

Non-Measurable Lesion, Absent

Datatype

text

Alias
UMLS CUI [1,1]
C1334988
UMLS CUI [1,2]
C0332197
Not Done
Beschrijving

Non-Measurable Lesion, Not Done

Datatype

text

Alias
UMLS CUI [1,1]
C1334988
UMLS CUI [1,2]
C1272696
Response Assessment Using WHO Criteria
Beschrijving

Response Assessment Using WHO Criteria

Alias
UMLS CUI-1
C0521982
UMLS CUI-2
C0220825
Was a response assessment performed?
Beschrijving

Response to treatment, Evaluation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0220825
Was this a confirmatory scan?
Beschrijving

Response to treatment, Evaluation, Confirmation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C0750484
Date of Lesion Assessment
Beschrijving

Lesion, Assessment Date

Datatype

date

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C2985720
Indicate the subject’s response for this tumor assessment, check only one
Beschrijving

Malignant Neoplasms, Evaluation, Disease Response

Datatype

text

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C1704632
Method of Assessment
Beschrijving

Response to treatment, Evaluation method

Datatype

text

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C2911685
Date of Clinical Assessment
Beschrijving

Response to treatment, Assessment Date, Clinical

Datatype

date

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C2985720
UMLS CUI [1,3]
C0205210
If ’Clinical Assessment’ is done, specify clinical symptoms of progression and method of assessment:
Beschrijving

Response to treatment, Evaluation, Clinical

Datatype

text

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C0205210
Local Laboratory - Haematology
Beschrijving

Local Laboratory - Haematology

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0474523
Lab ID
Beschrijving

Laboratory Identifier

Datatype

text

Alias
UMLS CUI [1]
C2986056
Laboratory name
Beschrijving

Performing laboratory name

Datatype

text

Alias
UMLS CUI [1]
C3258037
Address
Beschrijving

Performing Laboratory, Street Address

Datatype

text

Alias
UMLS CUI [1,1]
C1882331
UMLS CUI [1,2]
C1301826
Date sample taken
Beschrijving

Laboratory Procedures, Hematology finding, Sampling, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C0870078
UMLS CUI [1,4]
C0011008
Haematology Test
Beschrijving

Laboratory Procedures, Hematology finding

Datatype

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C0870078
UMLS CUI [1,4]
C0011008
Result
Beschrijving

Laboratory Procedures, Hematology finding, Result

Datatype

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0474523
UMLS CUI [1,3]
C1274040
Local Laboratory - Clinical Chemistry
Beschrijving

Local Laboratory - Clinical Chemistry

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0008000
Lab ID
Beschrijving

Laboratory Identifier

Datatype

text

Alias
UMLS CUI [1]
C2986056
Laboratory name
Beschrijving

Performing laboratory name

Datatype

text

Alias
UMLS CUI [1]
C3258037
Address
Beschrijving

Performing Laboratory, Street Address

Datatype

text

Alias
UMLS CUI [1,1]
C1882331
UMLS CUI [1,2]
C1301826
Date sample taken
Beschrijving

Laboratory Procedures, Chemistry, Clinical, Sampling, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0008000
UMLS CUI [1,3]
C0870078
UMLS CUI [1,4]
C0011008
Clinical Chemistry Test
Beschrijving

Laboratory Procedures, Chemistry, Clinical

Datatype

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0008000
Result
Beschrijving

Laboratory Procedures, Chemistry, Clinical, Result

Datatype

text

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0008000
UMLS CUI [1,3]
C1274040
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Similar models

End of Treatment

1 Formulieren
  1. StudyEvent: ODM
    1. End of Treatment
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
Vital Signs
C0518766 (UMLS CUI-1)
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Systolic Pressure
Item
Blood pressure - Systolic
integer
C0871470 (UMLS CUI [1])
Diastolic blood pressure
Item
Blood pressure - Diastolic
integer
C0871470 (UMLS CUI [1])
Heart rate
Item
Heart rate
integer
C0018810 (UMLS CUI [1])
Body Temperature
Item
Temperature
float
C0005903 (UMLS CUI [1])
Item Group
Lesion Assessment Using WHO Criteria - Indicator Lesions
C0221198 (UMLS CUI-1)
C1522602 (UMLS CUI-2)
C0220825 (UMLS CUI-3)
Lesion, Indicator, Numbers
Item
Lesion No.
integer
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
Lesion, Indicator, Organ, Code
Item
Anatomic Description - Organ Code
text
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,3])
C0805701 (UMLS CUI [1,4])
Lesion, Indicator, Location
Item
Anatomic Description - Lesion Location
text
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
Lesion, Indicator, Date in time
Item
Date
date
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Lesion, Indicator, Measurement method
Item
Can lesion be measured?
boolean
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C1299991 (UMLS CUI [1,3])
Lesion, Indicator, Diameter
Item
Diameter
integer
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
Lesion, Indicator, Lesion size
Item
Product
integer
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C0449453 (UMLS CUI [1,3])
Lesion, Indicator, Measurement method
Item
Method
text
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C1299991 (UMLS CUI [1,3])
Lesion, Indicator, Lesion Code
Item
Lesion Code
text
C0221198 (UMLS CUI [1,1])
C1522602 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
Item Group
Lesion Assessment Using WHO Criteria - Non-Measurable, Non-Evaluable Lesions
C1334988 (UMLS CUI-1)
C0220825 (UMLS CUI-2)
Non-Measurable Lesion, Numbers
Item
Lesion No.
integer
C1334988 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Item
Anatomic Description - Lesion Location
text
C1334988 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Non-Measurable Lesion, Location
Code List
Anatomic Description - Lesion Location
CL Item
Pericardial Effusion (1)
CL Item
Pleural Effusion (2)
CL Item
Ascites (3)
CL Item
Lymphangetic Metastases (4)
CL Item
Bone or Bone Marrow Metastases (5)
CL Item
Leptomeningeal Metastases (6)
Non-Measurable Lesion, Date in time
Item
Date
date
C1334988 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Non-Measurable Lesion, Present
Item
Present
text
C1334988 (UMLS CUI [1,1])
C0150312 (UMLS CUI [1,2])
Non-Measurable Lesion, Absent
Item
Absent
text
C1334988 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Non-Measurable Lesion, Not Done
Item
Not Done
text
C1334988 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
Item Group
Response Assessment Using WHO Criteria
C0521982 (UMLS CUI-1)
C0220825 (UMLS CUI-2)
Response to treatment, Evaluation
Item
Was a response assessment performed?
boolean
C0521982 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
Response to treatment, Evaluation, Confirmation
Item
Was this a confirmatory scan?
boolean
C0521982 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0750484 (UMLS CUI [1,3])
Lesion, Assessment Date
Item
Date of Lesion Assessment
date
C0221198 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
Item
Indicate the subject’s response for this tumor assessment, check only one
text
C0006826 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C1704632 (UMLS CUI [1,3])
Malignant Neoplasms, Evaluation, Disease Response
Code List
Indicate the subject’s response for this tumor assessment, check only one
CL Item
Complete Response (1)
CL Item
Partial Response (2)
CL Item
Stable Disease (3)
CL Item
Progressive Disease (4)
CL Item
Not Evaluable (5)
Item
Method of Assessment
text
C0521982 (UMLS CUI [1,1])
C2911685 (UMLS CUI [1,2])
Response to treatment, Evaluation method
Code List
Method of Assessment
CL Item
Lesion Assessment (1)
CL Item
Clinical Assessment (2)
Response to treatment, Assessment Date, Clinical
Item
Date of Clinical Assessment
date
C0521982 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
Response to treatment, Evaluation, Clinical
Item
If ’Clinical Assessment’ is done, specify clinical symptoms of progression and method of assessment:
text
C0521982 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
Item Group
Local Laboratory - Haematology
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
Laboratory Identifier
Item
Lab ID
text
C2986056 (UMLS CUI [1])
Performing laboratory name
Item
Laboratory name
text
C3258037 (UMLS CUI [1])
Performing Laboratory, Street Address
Item
Address
text
C1882331 (UMLS CUI [1,1])
C1301826 (UMLS CUI [1,2])
Laboratory Procedures, Hematology finding, Sampling, Date in time
Item
Date sample taken
date
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Item
Haematology Test
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Laboratory Procedures, Hematology finding
Code List
Haematology Test
CL Item
Haemoglobin (1)
CL Item
Haematocrit (2)
CL Item
Red Blood Cell (3)
CL Item
White Blood Cell (4)
CL Item
Platelet (5)
CL Item
Neutrophils (6)
CL Item
Bands (7)
CL Item
Lymphocytes (8)
CL Item
Monocytes (9)
CL Item
Eosinophils (10)
CL Item
Basophils (11)
Laboratory Procedures, Hematology finding, Result
Item
Result
text
C0022885 (UMLS CUI [1,1])
C0474523 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Item Group
Local Laboratory - Clinical Chemistry
C0022885 (UMLS CUI-1)
C0008000 (UMLS CUI-2)
Laboratory Identifier
Item
Lab ID
text
C2986056 (UMLS CUI [1])
Performing laboratory name
Item
Laboratory name
text
C3258037 (UMLS CUI [1])
Performing Laboratory, Street Address
Item
Address
text
C1882331 (UMLS CUI [1,1])
C1301826 (UMLS CUI [1,2])
Laboratory Procedures, Chemistry, Clinical, Sampling, Date in time
Item
Date sample taken
date
C0022885 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Item
Clinical Chemistry Test
text
C0022885 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
Laboratory Procedures, Chemistry, Clinical
Code List
Clinical Chemistry Test
CL Item
Sodium (1)
CL Item
Potassium (2)
CL Item
Chloride (3)
CL Item
Bicarbonate (4)
CL Item
Calcium (5)
CL Item
Phosphorus (6)
CL Item
Magnesium (7)
CL Item
Blood Urea Nitrogen (BUN) (8)
CL Item
Urea (9)
CL Item
Uric acid (10)
CL Item
Creatinine (11)
CL Item
LDH (12)
CL Item
Aspartate Aminotransferase (AST) (13)
CL Item
Alanine Transaminase (ALT) (14)
CL Item
Bilirubin (total) (15)
CL Item
Protein (total) (16)
CL Item
Albumin (17)
CL Item
Creatinine Clearance (calculated) (18)
CL Item
CA125 (19)
Laboratory Procedures, Chemistry, Clinical, Result
Item
Result
text
C0022885 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
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