ID

30039

Description

Study ID: 104450 Clinical Study ID: VEG104450 Study Title: This study is a non-randomized, open-label, multi-center Phase II study of GW786034 to evaluate the administration of oral GW786034 in subjects with ovarian cancer. Clinicaltrials.gov Identifier: NCT00281632 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: pazopanib Trade Name: Votrient Study Indication: Neoplasms, Ovarian CRF Pages: 722-853

Keywords

Versions (2)
  1. 5/3/18 5/3/18 -
  2. 5/4/18 5/4/18 - Julian Varghese
Copyright Holder

GlaxoSmithKline

Uploaded on

May 4, 2018

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Oral GW786034 treatment for ovarian cancer NCT00281632

English

Visit description: Treatment Period 1. Day 1

1 forms  
Header
Description

Header

Alias
UMLS CUI-1
C1320722
Subject Identifier
Description

Subject Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Visit Date
Description

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
Centre Number
Description

Centre Number

Data type

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Vital signs
Description

Vital signs

Heart rate
Description

Heart rate

Data type

integer

Measurement units
  • bpm
Alias
UMLS CUI [1]
C0018810
bpm
Blood pressure, systolic
Description

Blood pressure, systolic

Data type

integer

Measurement units
  • mm[Hg]
Alias
UMLS CUI [1]
C0871470
mm[Hg]
Blood pressure, diastolic
Description

Blood pressure, diastolic

Data type

integer

Measurement units
  • mm[Hg]
Alias
UMLS CUI [1]
C0428883
mm[Hg]
Temperature
Description

Temperature

Data type

float

Measurement units
  • ° C
Alias
UMLS CUI [1]
C0039476
° C
ECOG Performance Status
Description

ECOG Performance Status

Alias
UMLS CUI-1
C1520224
ECOG
Description

This section contained Clinical Outcome Assessment data collection questionnaires or indices, which are protected by copyright laws and therefore have been excluded.

Data type

integer

Alias
UMLS CUI [1]
C1520224
Electronically transferred laboratory data - CA-125
Description

Electronically transferred laboratory data - CA-125

Alias
UMLS CUI-1
C0200345
UMLS CUI-3
C0022885
UMLS CUI-5
C0201549
Date sample taken
Description

Date sample taken CA-125

Data type

date

Alias
UMLS CUI [1,1]
C1302413
UMLS CUI [1,2]
C0201549
Physical examination
Description

Physical examination

Alias
UMLS CUI-1
C0031809
Has a physical examination been performed on the subject?
Description

physical examination

Data type

boolean

Alias
UMLS CUI [1]
C0031809
Examination Status
Description

Examination Status

Data type

integer

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C0449438
If abnormal record below
Description

abnormal physical examination

Data type

text

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C0459424
Concomitant Medications
Description

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Adverse Events
Description

Adverse Events

Alias
UMLS CUI-1
C0877248
Local Laboratory - Haematology
Description

Local Laboratory - Haematology

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

Lab ID

Data type

text

Alias
UMLS CUI [1,1]
C0022877
UMLS CUI [1,2]
C0600091
Laboratory name
Description

Laboratory name

Data type

text

Alias
UMLS CUI [1]
C1882331
Address
Description

Laboratory Address

Data type

text

Alias
UMLS CUI [1]
C3262820
Date Sample taken Haematology
Description

Date Sample taken Haematology

Data type

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0018941
UMLS CUI [1,3]
C1302413
Haematocrit (HCT)
Description

Haematocrit (HCT)

Data type

float

Alias
UMLS CUI [1]
C0018935
Haemoglobin (Hb)
Description

Haemoglobin (Hb)

Data type

float

Alias
UMLS CUI [1]
C0518015
Platelet count (absolute)
Description

Platelet count (absolute)

Data type

float

Alias
UMLS CUI [1]
C0032181
White blood cell count (WBC) (Absolute)
Description

White blood cell count (WBC) (Absolute)

Data type

float

Alias
UMLS CUI [1]
C0023508
Neutrophil count (absolute)
Description

Neutrophil count (absolute)

Data type

float

Alias
UMLS CUI [1]
C0948762
Lymphocyte count (absolute)
Description

Lymphocyte count (absolute)

Data type

float

Alias
UMLS CUI [1]
C3544087
Local Laboratory - Clinical Chemistry
Description

Local Laboratory - Clinical Chemistry

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

Lab ID

Data type

integer

Alias
UMLS CUI [1,1]
C0022877
UMLS CUI [1,2]
C0600091
Laboratory name
Description

Laboratory name

Data type

text

Alias
UMLS CUI [1]
C1882331
Address
Description

Laboratory Address

Data type

text

Alias
UMLS CUI [1]
C3262820
Date sample taken clinical chemistry
Description

Date sample taken

Data type

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0008000
UMLS CUI [1,3]
C1302413
Alkaline phosphatase
Description

Alkaline phosphatase

Data type

float

Alias
UMLS CUI [1]
C0201850
ALT (SGPT)
Description

ALT (SGPT)

Data type

float

Alias
UMLS CUI [1]
C0201836
AST (SGOT)
Description

AST (SGOT)

Data type

float

Alias
UMLS CUI [1]
C0201899
Albumin
Description

Albumin

Data type

float

Alias
UMLS CUI [1]
C0201838
Total bilirubin
Description

Total bilirubin

Data type

float

Alias
UMLS CUI [1]
C0201913
Blood Urea Nitrogen
Description

BUN

Data type

float

Alias
UMLS CUI [1]
C0005845
Calcium
Description

Calcium

Data type

float

Alias
UMLS CUI [1]
C0201925
Serum Creatinine
Description

Serum Creatinine

Data type

float

Alias
UMLS CUI [1]
C0201976
Glucose (fasting)
Description

Glucose (fasting)

Data type

float

Alias
UMLS CUI [1]
C0583513
LDH
Description

LDH

Data type

float

Alias
UMLS CUI [1]
C0202113
Potassium
Description

Potassium

Data type

float

Alias
UMLS CUI [1]
C0202194
Sodium
Description

Sodium

Data type

float

Alias
UMLS CUI [1]
C0337443
Urinalysis
Description

Urinalysis

Alias
UMLS CUI-1
C0042014
Date sample taken
Description

Date sample taken

Data type

date

Alias
UMLS CUI [1]
C1302413
Laboratory name
Description

Laboratory name

Data type

text

Alias
UMLS CUI [1]
C3258037
Address
Description

Address

Data type

text

Alias
UMLS CUI [1,1]
C1442065
UMLS CUI [1,2]
C0022877
UPC ratio
Description

UPC ratio

Data type

float

Alias
UMLS CUI [1,1]
C1524119
UMLS CUI [1,2]
C0033684
UMLS CUI [1,3]
C1522609
Lab ID
Description

Lab ID

Data type

text

Alias
UMLS CUI [1,1]
C0022877
UMLS CUI [1,2]
C0600091
Tumour Tissue Sample Collection
Description

Tumour Tissue Sample Collection

Alias
UMLS CUI-1
C0475358
UMLS CUI-2
C0005558
Has a tissue sample been collected?
Description

tumor tissue collection

Data type

boolean

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C0005558
If No, tick appropriate reason
Description

no biopsy reason

Data type

text

Alias
UMLS CUI [1,1]
C0005558
UMLS CUI [1,2]
C1272696
UMLS CUI [1,3]
C0392360
If other, please specify
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394
Sample Collection
Description

Sample Collection

Data type

text

Alias
UMLS CUI [1]
C1547864
Preservation Method
Description

Biopsy sample preservation method

Data type

text

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C1514402
Form Type
Description

tissue sample form type

Data type

text

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C0332479
Type of Tissue Biopsy
Description

Type of Tissue Biopsy

Data type

text

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C0005558
UMLS CUI [1,3]
C0332307
Organ Code
Description

Organ code

Data type

text

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0805701
Tissue Source
Description

Tissue Source

Data type

text

Alias
UMLS CUI [1,1]
C0475358
UMLS CUI [1,2]
C0449416
UMLS CUI [1,3]
C0678257
Date Biopsy Taken
Description

Date Biopsy Taken

Data type

date

Alias
UMLS CUI [1,1]
C0005558
UMLS CUI [1,2]
C1302413
Time Biopsy Taken
Description

Time Biopsy Taken

Data type

partialDatetime

Alias
UMLS CUI [1,1]
C0005558
UMLS CUI [1,2]
C0200345
UMLS CUI [1,3]
C0040223
Consent for tumour genetic research
Description

Consent for tumour genetic research

Alias
UMLS CUI-1
C0586888
UMLS CUI-2
C0243064
Has consent been obtained for tumour genetic research?
Description

consent for tumour genetic research

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0243064
If yes, record date consent obtained
Description

date of informed consent

Data type

date

Alias
UMLS CUI [1]
C2985782
If no, tick one reason
Description

reason no consent given

Data type

text

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1705492
if other, specify
Description

other reason

Data type

text

Alias
UMLS CUI [1]
C3840932
Withdrawal of consent
Description

Withdrawal of consent

Has subject withdrawn consent for tumour genetic research?
Description

Withdrawal of consent

Data type

boolean

Alias
UMLS CUI [1,1]
C1707492
UMLS CUI [1,2]
C0243064
If Yes, record the date informed consent withdrawn for tumour genetic research
Description

Date of withdrawal of consent

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1707492
UMLS CUI [1,3]
C0243064
Sample Destruction
Description

Sample Destruction

Alias
UMLS CUI-1
C1948029
UMLS CUI-2
C0475358
Has a request been made for tumour genetics tissue sample destruction?
Description

Request made for destruction of tumour sample

Data type

boolean

Alias
UMLS CUI [1,1]
C1272683
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C0178913
If yes, tick one reason
Description

Reason for tumour sample destruction

Data type

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C1948029
UMLS CUI [1,3]
C0475358
If other, please specify
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394
Biomarker sample(s)
Description

Biomarker sample(s)

Alias
UMLS CUI-1
C0005516
Sample Type
Description

Biomarker Sample Type

Data type

text

Alias
UMLS CUI [1,1]
C2347029
UMLS CUI [1,2]
C0005516
Has sample been collected?
Description

Biomarker sample collected

Data type

boolean

Alias
UMLS CUI [1,1]
C0005516
UMLS CUI [1,2]
C0200345
If No, provide reason
Description

If no, reason

Data type

text

Alias
UMLS CUI [1]
C0681841
Date sample taken
Description

Date sample taken

Data type

date

Alias
UMLS CUI [1]
C1302413
Time sample taken
Description

Time sample taken

Data type

partialDatetime

Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0200345
Back to the top of the page

Similar models

Visit description: Treatment Period 1. Day 1

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Header
C1320722 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Centre Number
Item
Centre Number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Item Group
Vital signs
Heart rate
Item
Heart rate
integer
C0018810 (UMLS CUI [1])
Blood pressure, systolic
Item
Blood pressure, systolic
integer
C0871470 (UMLS CUI [1])
Blood pressure, diastolic
Item
Blood pressure, diastolic
integer
C0428883 (UMLS CUI [1])
Temperature
Item
Temperature
float
C0039476 (UMLS CUI [1])
Item Group
ECOG Performance Status
C1520224 (UMLS CUI-1)
ECOG
Item
ECOG
integer
C1520224 (UMLS CUI [1])
Item Group
Electronically transferred laboratory data - CA-125
C0200345 (UMLS CUI-1)
C0022885 (UMLS CUI-3)
C0201549 (UMLS CUI-5)
Date sample taken CA-125
Item
Date sample taken
date
C1302413 (UMLS CUI [1,1])
C0201549 (UMLS CUI [1,2])
Item Group
Physical examination
C0031809 (UMLS CUI-1)
physical examination
Item
Has a physical examination been performed on the subject?
boolean
C0031809 (UMLS CUI [1])
Item
Examination Status
integer
C0031809 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Examination Status
Code List
Examination Status
CL Item
Normal (N)
(Comment:en)
CL Item
Abnormal (please specify) (A)
(Comment:en)
abnormal physical examination
Item
If abnormal record below
text
C0031809 (UMLS CUI [1,1])
C0459424 (UMLS CUI [1,2])
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Item Group
Adverse Events
C0877248 (UMLS CUI-1)
Item Group
Local Laboratory - Haematology
C0474523 (UMLS CUI-1)
C0022885 (UMLS CUI-2)
Lab ID
Item
Lab ID
text
C0022877 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Laboratory name
Item
Laboratory name
text
C1882331 (UMLS CUI [1])
Laboratory Address
Item
Address
text
C3262820 (UMLS CUI [1])
Date Sample taken Haematology
Item
Date Sample taken Haematology
date
C0005834 (UMLS CUI [1,1])
C0018941 (UMLS CUI [1,2])
C1302413 (UMLS CUI [1,3])
Haematocrit (HCT)
Item
Haematocrit (HCT)
float
C0018935 (UMLS CUI [1])
Haemoglobin (Hb)
Item
Haemoglobin (Hb)
float
C0518015 (UMLS CUI [1])
Platelet count (absolute)
Item
Platelet count (absolute)
float
C0032181 (UMLS CUI [1])
White blood cell count (WBC) (Absolute)
Item
White blood cell count (WBC) (Absolute)
float
C0023508 (UMLS CUI [1])
Neutrophil count (absolute)
Item
Neutrophil count (absolute)
float
C0948762 (UMLS CUI [1])
Lymphocyte count (absolute)
Item
Lymphocyte count (absolute)
float
C3544087 (UMLS CUI [1])
Item Group
Local Laboratory - Clinical Chemistry
C0008000 (UMLS CUI-1)
C0022885 (UMLS CUI-2)
Lab ID
Item
Lab ID
integer
C0022877 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Laboratory name
Item
Laboratory name
text
C1882331 (UMLS CUI [1])
Laboratory Address
Item
Address
text
C3262820 (UMLS CUI [1])
Date sample taken
Item
Date sample taken clinical chemistry
date
C0005834 (UMLS CUI [1,1])
C0008000 (UMLS CUI [1,2])
C1302413 (UMLS CUI [1,3])
Alkaline phosphatase
Item
Alkaline phosphatase
float
C0201850 (UMLS CUI [1])
ALT (SGPT)
Item
ALT (SGPT)
float
C0201836 (UMLS CUI [1])
AST (SGOT)
Item
AST (SGOT)
float
C0201899 (UMLS CUI [1])
Albumin
Item
Albumin
float
C0201838 (UMLS CUI [1])
Total bilirubin
Item
Total bilirubin
float
C0201913 (UMLS CUI [1])
BUN
Item
Blood Urea Nitrogen
float
C0005845 (UMLS CUI [1])
Calcium
Item
Calcium
float
C0201925 (UMLS CUI [1])
Serum Creatinine
Item
Serum Creatinine
float
C0201976 (UMLS CUI [1])
Glucose (fasting)
Item
Glucose (fasting)
float
C0583513 (UMLS CUI [1])
LDH
Item
LDH
float
C0202113 (UMLS CUI [1])
Potassium
Item
Potassium
float
C0202194 (UMLS CUI [1])
Sodium
Item
Sodium
float
C0337443 (UMLS CUI [1])
Item Group
Urinalysis
C0042014 (UMLS CUI-1)
Date sample taken
Item
Date sample taken
date
C1302413 (UMLS CUI [1])
Laboratory name
Item
Laboratory name
text
C3258037 (UMLS CUI [1])
Address
Item
Address
text
C1442065 (UMLS CUI [1,1])
C0022877 (UMLS CUI [1,2])
UPC ratio
Item
UPC ratio
float
C1524119 (UMLS CUI [1,1])
C0033684 (UMLS CUI [1,2])
C1522609 (UMLS CUI [1,3])
Lab ID
Item
Lab ID
text
C0022877 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Item Group
Tumour Tissue Sample Collection
C0475358 (UMLS CUI-1)
C0005558 (UMLS CUI-2)
tumor tissue collection
Item
Has a tissue sample been collected?
boolean
C0475358 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
Item
If No, tick appropriate reason
text
C0005558 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
no biopsy reason
Code List
If No, tick appropriate reason
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other, specify (OT)
Other
Item
If other, please specify
text
C0205394 (UMLS CUI [1])
Item
Sample Collection
text
C1547864 (UMLS CUI [1])
Sample Collection
Code List
Sample Collection
CL Item
Derived During Study (1)
CL Item
Archieved (2)
Item
Preservation Method
text
C0475358 (UMLS CUI [1,1])
C1514402 (UMLS CUI [1,2])
Biopsy sample preservation method
Code List
Preservation Method
CL Item
FFPE (1)
CL Item
Fresh-frozen (2)
Item
Form Type
text
C0475358 (UMLS CUI [1,1])
C0332479 (UMLS CUI [1,2])
tissue sample form type
Code List
Form Type
CL Item
Block (1)
CL Item
Slides (2)
Item
Type of Tissue Biopsy
text
C0475358 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
Type of Tissue Biopsy
Code List
Type of Tissue Biopsy
CL Item
Core (1)
CL Item
Excisional (2)
CL Item
FNA (fine needle aspiration) (3)
CL Item
Punch (4)
CL Item
Other, specify (OT)
Item
Organ Code
text
C0678852 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
Organ code
Code List
Organ Code
CL Item
Abdomen/abdominal wall  (AB)
CL Item
Liver  (LV)
CL Item
Lymph nodes  (LN)
CL Item
Ovary  (OV)
CL Item
Peritoneum (PM)
CL Item
Spleen (SP)
CL Item
Small intestine (SI)
CL Item
Other, specify (CT)
Item
Tissue Source
text
C0475358 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,3])
Tissue Source
Code List
Tissue Source
CL Item
Primary (1)
CL Item
Metastasic (2)
CL Item
Unknown (U)
Date Biopsy Taken
Item
Date Biopsy Taken
date
C0005558 (UMLS CUI [1,1])
C1302413 (UMLS CUI [1,2])
Time Biopsy Taken
Item
Time Biopsy Taken
partialDatetime
C0005558 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item Group
Consent for tumour genetic research
C0586888 (UMLS CUI-1)
C0243064 (UMLS CUI-2)
consent for tumour genetic research
Item
Has consent been obtained for tumour genetic research?
boolean
C0021430 (UMLS CUI [1,1])
C0243064 (UMLS CUI [1,2])
date of informed consent
Item
If yes, record date consent obtained
date
C2985782 (UMLS CUI [1])
Item
If no, tick one reason
text
C0566251 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,3])
reason no consent given
Code List
If no, tick one reason
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other, specify (3)
other reason
Item
if other, specify
text
C3840932 (UMLS CUI [1])
Item Group
Withdrawal of consent
Withdrawal of consent
Item
Has subject withdrawn consent for tumour genetic research?
boolean
C1707492 (UMLS CUI [1,1])
C0243064 (UMLS CUI [1,2])
Date of withdrawal of consent
Item
If Yes, record the date informed consent withdrawn for tumour genetic research
date
C0011008 (UMLS CUI [1,1])
C1707492 (UMLS CUI [1,2])
C0243064 (UMLS CUI [1,3])
Item Group
Sample Destruction
C1948029 (UMLS CUI-1)
C0475358 (UMLS CUI-2)
Request made for destruction of tumour sample
Item
Has a request been made for tumour genetics tissue sample destruction?
boolean
C1272683 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
Item
If yes, tick one reason
text
C0392360 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0475358 (UMLS CUI [1,3])
Reason for tumour sample destruction
Code List
If yes, tick one reason
CL Item
Subject withdrew consent for tumour genetic research (4)
CL Item
Other, specify (OT)
Other
Item
If other, please specify
text
C0205394 (UMLS CUI [1])
Item Group
Biomarker sample(s)
C0005516 (UMLS CUI-1)
Item
Sample Type
text
C2347029 (UMLS CUI [1,1])
C0005516 (UMLS CUI [1,2])
Biomarker Sample Type
Code List
Sample Type
CL Item
Platelet poor plasma  (1)
CL Item
Serum  (2)
CL Item
Bone marrow aspirate  (3)
CL Item
Whole blood  (5)
CL Item
Urine  (6)
CL Item
Mucus  (7)
CL Item
Plasma (8)
CL Item
Saliva (9)
CL Item
Stool (10)
CL Item
Ascites (11)
CL Item
Cerebral spinal fluid (12)
CL Item
Pleural fluid (13)
CL Item
Buccal swab (15)
Biomarker sample collected
Item
Has sample been collected?
boolean
C0005516 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
Item
If No, provide reason
text
C0681841 (UMLS CUI [1])
If no, reason
Code List
If No, provide reason
CL Item
Subject not asked by Investigator (2)
CL Item
Other, specify (OT)
Date sample taken
Item
Date sample taken
date
C1302413 (UMLS CUI [1])
Time sample taken
Item
Time sample taken
partialDatetime
C0040223 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

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