Experimental drug, Medication administered
Item
Was study drug given?
boolean
C0304229 (UMLS CUI [1,1])
C0806914 (UMLS CUI [1,2])
Pharmaceutical Preparation; Dosage; Date in time; Time
Item
Date and Time of Dosing
datetime
C0013227 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Clinical Trial Subject Unique Identifier
Item
Treatment Number
integer
C2348585 (UMLS CUI [1])
Administration procedure, Not Done, Indication; Administration procedure, Late, Indication
Item
Indicate reason if not done or outside time window
text
C1533734 (UMLS CUI [1,1])
C1272696 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C1533734 (UMLS CUI [2,1])
C0205087 (UMLS CUI [2,2])
C0392360 (UMLS CUI [2,3])
Item
Day 3
text
C0474523 (UMLS CUI [1])
CL Item
Not done (Not done)
CL Item
Same laboratory as recorded before (Same laboratory as recorded before)
Hematology finding, Performing Laboratory
Item
Laboratory Name/City
text
C0474523 (UMLS CUI [1,1])
C1882331 (UMLS CUI [1,2])
Hematology finding; Sampling; Date in time; Time
Item
Date and Time of Sampling
datetime
C0474523 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Test
text
C0474523 (UMLS CUI [1,1])
C0018941 (UMLS CUI [1,2])
CL Item
Platelet (Platelet)
CL Item
Hemoglobin (Hemoglobin)
Hematology finding; Numerical Value
Item
Value
float
C0474523 (UMLS CUI [1,1])
C1522609 (UMLS CUI [1,2])
Item
Unit
text
C0474523 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
Hematology finding; Unit, other
Item
If other unit, specify
text
C0474523 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Biochemistry; Performing Laboratory
Item
Laboratory Name/City
text
C0005477 (UMLS CUI [1,1])
C1882331 (UMLS CUI [1,2])
Biochemistry; Sampling; Date in time; Time
Item
Date and Time of Sampling
datetime
C0005477 (UMLS CUI [1,1])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Test
text
C1655775 (UMLS CUI [1])
CL Item
Creatinine (Creatinine)
CL Item
Total Bilirubin (Total Bilirubin)
Biochemistry; Numerical Value
Item
Value
float
C0005477 (UMLS CUI [1,1])
C1522609 (UMLS CUI [1,2])
Item
Unit
text
C0005477 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
Item
If other unit, specify
text
C0005477 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Code List
If other unit, specify
Venography
Item
Not done
boolean
C0031545 (UMLS CUI [1])
Venography, Bilateral
Item
Bilateral
boolean
C0031545 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
Venography, Bilateral, Date in time
Item
Bilateral, Date performed
date
C0031545 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Venography, Structure of left lower leg
Item
Left Leg
boolean
C0031545 (UMLS CUI [1,1])
C0230443 (UMLS CUI [1,2])
Venography, Structure of left lower leg, Date in time
Item
Left Leg, Date performed
date
C0031545 (UMLS CUI [1,1])
C0230443 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Venography, Structure of right lower leg
Item
Right Leg
boolean
C0031545 (UMLS CUI [1,1])
C0230442 (UMLS CUI [1,2])
Venography, Structure of right lower leg, Date in time
Item
Right Leg, Date performed
date
C0031545 (UMLS CUI [1,1])
C0230442 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
If NOT BILATERAL or NOT DONE, tick the primary reason.
text
C0031545 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
Code List
If NOT BILATERAL or NOT DONE, tick the primary reason.
CL Item
Failed venous access (Failed venous access)
CL Item
Subject refused/withdrew consent (Subject refused/withdrew consent)
CL Item
Subject amputee (Subject amputee)
CL Item
Other, specify (Other, specify)
Venography; Result; Pharmaceutical Preparations
Item
As a result of this venography, was medication given to treat DVT?
boolean
C0031545 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
Intermittent Pneumatic Compression Therapy, Knee, High
Item
Intermittent Pneumatic Compression, knee-high
boolean
C1998430 (UMLS CUI [1,1])
C0022742 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,3])
Intermittent Pneumatic Compression Therapy, Thigh, High
Item
Intermittent Pneumatic Compression, thigh-high
boolean
C1998430 (UMLS CUI [1,1])
C0039866 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,3])
Intermittent Pneumatic Compression Therapy; Start Date
Item
Compression Therapy; Date of start
date
C1998430 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Intermittent Pneumatic Compression Therapy; Removing; Date in time
Item
Compression Therapy; Date of removal
date
C1998430 (UMLS CUI [1,1])
C1883720 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Compression stockings
Item
Did the subject wear elastic stockings (TED HOSE) for thrombosis prevention during the treatment period?
boolean
C0038348 (UMLS CUI [1])
Compression stockings; Start date
Item
Date of start
date
C0038348 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Compression stockings; Removing, Date in time
Item
Date of removal
date
C0038348 (UMLS CUI [1,1])
C1883720 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Physical therapy
Item
Did the subject receive physical therapy during the treatment period?
boolean
C0949766 (UMLS CUI [1])
Ambulate, Start date
Item
What day did the subject first ambulate?
date
C4036205 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])