ID

45880

Beskrivning

CombiCaRe Protocol of a prospective, monocentric phase I/II feasibility study investigating the safety of multimodality treatment with a combination of intraoperative chemotherapy and surgical resection in locally confined or borderline resectable pancreatic cancer: the combiCaRe study. Roth S, Springfeld C, Diener MK, Tjaden C, Knebel P, Klaiber U, Michalski CW, Mieth M, Jäger D, Büchler MW, Hackert T.

Nyckelord

  1. 2023-11-10 2023-11-10 - Nelly Zental
Rättsinnehavare

Roth S, Springfeld C, Diener MK, Tjaden C, Knebel P, Klaiber U, Michalski CW, Mieth M, Jäger D, Büchler MW, Hackert T.

Uppladdad den

10 november 2023

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :


Inga kommentarer

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

CombiCaRe study

Intervention

  1. StudyEvent: combicare trial
    1. Screening
    2. Intervention
    3. POD 3
    4. POD 7
    5. POD 14 / Discharge
    6. POD 30
    7. POD 60/Discontinuation
    8. Signature
  2. StudyEvent: Readmission To Hospital
    1. Readmission To Hospital
  3. StudyEvent: Adverse Events
    1. Adverse Events
  4. StudyEvent: Concomitant Medication
    1. Concomitant Medication
  5. StudyEvent: Protocol Violation
    1. Protocol violation
5-FU treatment
Beskrivning

5-FU treatment

Alias
UMLS CUI [1,1]
C0016360
UMLS CUI [1,2]
C1533734
Start of 5-FU chemotherapy (date)
Beskrivning

Start 5-FU date

Datatyp

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0016360
UMLS CUI [1,3]
C0392920
Start of 5-FU chemotherapy (time)
Beskrivning

Start 5-FU time

Datatyp

time

Alias
UMLS CUI [1,1]
C1301880
UMLS CUI [1,2]
C0016360
UMLS CUI [1,3]
C0392920
Planned dose of 5-FU chemotherapy
Beskrivning

Planned dose 5-FU

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1,1]
C2826283
mg
Modification of planned 5-FU dose?
Beskrivning

Modification 5-FU dose

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1707811
Reason for 5-FU dose modification
Beskrivning

Reason modification

Datatyp

text

Alias
UMLS CUI [1,1]
C0392360
If other, please specify
Beskrivning

specify reason

Datatyp

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C1521902
Dose administered
Beskrivning

Dose administered

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1,1]
C2348343
mg
End of 5-FU chemotherapy (date)
Beskrivning

End 5-FU date

Datatyp

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0016360
UMLS CUI [1,3]
C0392920
End of 5-FU chemotherapy (time)
Beskrivning

End 5-FU time

Datatyp

time

Alias
UMLS CUI [1,1]
C1522314
UMLS CUI [1,2]
C0016360
UMLS CUI [1,3]
C0392920
Calcium folinate and Granisetron treatment
Beskrivning

Calcium folinate and Granisetron treatment

Alias
UMLS CUI [1,1]
C0061863
UMLS CUI [2,1]
C0023413
Modification of planned Calcium folinate treatment?
Beskrivning

Modification Calcium folinate

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1299575
UMLS CUI [1,2]
C0023413
Reason for Calcium folinate dose modification
Beskrivning

Reason modification

Datatyp

text

Alias
UMLS CUI [1,1]
C0392360
If other, please specify
Beskrivning

specify reason

Datatyp

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C1521902
Modification of planned Granisetron treatment?
Beskrivning

Modification Granisetron

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1299575
UMLS CUI [1,2]
C0061863
If yes, please specify discrepancy
Beskrivning

specify discrepancy

Datatyp

text

Alias
UMLS CUI [1,1]
C1521902
UMLS CUI [1,2]
C3840684)
Surgery
Beskrivning

Surgery

Alias
UMLS CUI [1,1]
C0543467
Date of surgery
Beskrivning

Date of surgery

Datatyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0543467
Intraoperative re-evaluation of resectability
Beskrivning

Intraoperative re-evaluation of resectability

Alias
UMLS CUI [1,1]
C0456904
UMLS CUI [1,2]
C0681840
UMLS CUI [1,3]
C5396338
Result of intraoperative re-evaluation of resectability
Beskrivning

Result re-evaluation

Datatyp

text

Alias
UMLS CUI [1,1]
C1274040
UMLS CUI [1,2]
C0456904
UMLS CUI [1,3]
C0681840
UMLS CUI [1,4]
C5396338
Exclusion of liver metastasis
Beskrivning

Exclusion of liver metastasis

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0494165
Exclusion of peritoneal carcinomatosis
Beskrivning

Exclusion of peritoneal carcinomatosis

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0346990
Exclusion of superior mesenteric / hepatic artery encasement
Beskrivning

Exclusion of superior mesenteric / hepatic artery encasement

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C4524504
UMLS CUI [1,3]
C0019145
UMLS CUI [1,4]
C0162861
Tumor location (pancreas)
Beskrivning

Tumor location (pancreas)

Alias
UMLS CUI [1,1]
C2063875
uncinate process
Beskrivning

uncinate process

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0227580
head
Beskrivning

head

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0227579
body
Beskrivning

body

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0227582
tail
Beskrivning

tail

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0227590
Surgery Details
Beskrivning

Surgery Details

Alias
UMLS CUI [1,1]
C5204320
Start skin incision (time)
Beskrivning

Start

Datatyp

time

Alias
UMLS CUI [1,1]
C0191279
UMLS CUI [1,2]
C1301880
End of surgery (time)
Beskrivning

End

Datatyp

time

Alias
UMLS CUI [1,1]
C1522314
UMLS CUI [1,2]
C0543467
Performed surgical intervention
Beskrivning

surgical intervention

Datatyp

text

Alias
UMLS CUI [1,1]
C4035998
If other, please specify
Beskrivning

specify surgical intervention

Datatyp

text

Alias
UMLS CUI [1,1]
C1521902
Additional resections
Beskrivning

Additional resections

Alias
UMLS CUI [1,1]
C1524062
UMLS CUI [1,2]
C0015252
Vascular (venous) resections and reconstructions
Beskrivning

Vascular resections

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0189617
Vascular (venous) resections and reconstructions
Beskrivning

Vascular (venous) resections and reconstructions

Alias
UMLS CUI [1,1]
C0189617
portal venous resection
Beskrivning

portal venous resection

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0226727
UMLS CUI [1,2]
C00152526
VMS resection
Beskrivning

VMS resection

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0226742
UMLS CUI [1,2]
C0015252
other
Beskrivning

other

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0205394
If other vascular resection, please specify
Beskrivning

specify vascular resections

Datatyp

text

Alias
UMLS CUI [1,1]
C1521902
Additional resections
Beskrivning

Additional resections

Alias
UMLS CUI [1,1]
C1524062
UMLS CUI [1,2]
C0015252
Additional resections
Beskrivning

Additional resections

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1706712
UMLS CUI [1,2]
C0015252
If yes, please specify additional resections
Beskrivning

If yes, please specify additional resections

Alias
UMLS CUI [1,1]
C1521902
lymphadenectomy
Beskrivning

lymphadenectomy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0024203
extrapancreatic resections
Beskrivning

extrapancreatic resections

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0015252
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C0030274
other
Beskrivning

other

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0205394
If extrapancreatic resection, please specify
Beskrivning

specify extrapancreatic resection

Datatyp

text

Alias
UMLS CUI [1,1]
C1521902
If other, please specify
Beskrivning

specify other

Datatyp

text

Alias
UMLS CUI [1,1]
C1521902
Blood loss and Transfusion
Beskrivning

Blood loss and Transfusion

Alias
UMLS CUI [1,1]
C3163616
UMLS CUI [1,2]
C0005841
Intraoperative blood loss (as estimated from the anesthesia protocol)
Beskrivning

Intraoperative blood loss

Datatyp

boolean

Alias
UMLS CUI [1,1]
C5208110
If yes, please specify
Beskrivning

specify blood loss

Datatyp

float

Måttenheter
  • ml
Alias
UMLS CUI [1,1]
C1521902
ml
Blood transfusion
Beskrivning

Blood transfusion

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0005841
Type of blood transfusion
Beskrivning

Type of blood transfusion

Alias
UMLS CUI [1,1]
C5420007
red blood cell concentrates
Beskrivning

red blood cell concentrates

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0086252
Volume of red blood cell concentrates
Beskrivning

Volume red blood cell concentrates

Datatyp

float

Måttenheter
  • ml
Alias
UMLS CUI [1,1]
C0086252
UMLS CUI [1,2]
C1264726
ml
fresh frozen plasma (FFP)
Beskrivning

fresh frozen plasma (FFP)

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1293883
Volume of fresh frozen plasma (FFP)
Beskrivning

Volume FFPs

Datatyp

float

Måttenheter
  • ml
Alias
UMLS CUI [1,1]
C1293883
UMLS CUI [1,2]
C1264726
ml
thrombocyte concentrates
Beskrivning

thrombocyte concentrates

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1293886
Volume of thrombocyte concentrates
Beskrivning

Volume thrombocyte concentrates

Datatyp

float

Måttenheter
  • ml
Alias
UMLS CUI [1,1]
C1293886
UMLS CUI [1,2]
C1264726
ml
Translational Studies
Beskrivning

Translational Studies

Alias
UMLS CUI [1,1]
C1519620
Blood sample taken (portal vein and peripheral vein)
Beskrivning

Blood sample

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1277698
UMLS CUI [1,2]
C2324289
UMLS CUI [1,3]
C5401001
Bone marrow sample taken
Beskrivning

Bone marrow

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0005954
Tumor tissue sample taken
Beskrivning

Tumor tissue

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0475358
Concomitant Medication
Beskrivning

Concomitant Medication

Alias
UMLS CUI [1,1]
C2347852
Any changes in Concomitant Medication (since last visit)?
Beskrivning

changes in Concomitant Medication

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3872643
UMLS CUI [1,2]
C0392747
If yes, please fill out eForm 'Concomitant Medication'
Beskrivning

If yes, please fill out eForm 'Concomitant Medication'

Alias
UMLS CUI [1,1]
C3273494
UMLS CUI [1,2]
C2347852
Adverse Events
Beskrivning

Adverse Events

Alias
UMLS CUI [1,1]
C0877248
Any Adverse Events occurred since last visit?
Beskrivning

Adverse Events occurred

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3872643
If yes, please fill out eForm 'Adverse Events'
Beskrivning

If yes, please fill out eForm 'Adverse Events'

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C3273494
Protocol violations
Beskrivning

Protocol violations

Alias
UMLS CUI [1,1]
C1709750
Any protocol violations occurred since last visit?
Beskrivning

protocol violations occurred

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3872643
If yes, please fill out eForm 'Protocol Violation'
Beskrivning

If yes, please fill out eForm 'Protocol Violation'

Alias
UMLS CUI [1,1]
C3273494

Similar models

Intervention

  1. StudyEvent: combicare trial
    1. Screening
    2. Intervention
    3. POD 3
    4. POD 7
    5. POD 14 / Discharge
    6. POD 30
    7. POD 60/Discontinuation
    8. Signature
  2. StudyEvent: Readmission To Hospital
    1. Readmission To Hospital
  3. StudyEvent: Adverse Events
    1. Adverse Events
  4. StudyEvent: Concomitant Medication
    1. Concomitant Medication
  5. StudyEvent: Protocol Violation
    1. Protocol violation
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
5-FU treatment
C0016360 (UMLS CUI [1,1])
C1533734 (UMLS CUI [1,2])
Start 5-FU date
Item
Start of 5-FU chemotherapy (date)
date
C0808070 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Start 5-FU time
Item
Start of 5-FU chemotherapy (time)
time
C1301880 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Planned dose 5-FU
Item
Planned dose of 5-FU chemotherapy
float
C2826283 (UMLS CUI [1,1])
Modification 5-FU dose
Item
Modification of planned 5-FU dose?
boolean
C1707811 (UMLS CUI [1,1])
Item
Reason for 5-FU dose modification
text
C0392360 (UMLS CUI [1,1])
Code List
Reason for 5-FU dose modification
CL Item
toxicity (1)
C0013221 (UMLS CUI [1,1])
CL Item
allergy (2)
C0013182 (UMLS CUI [1,1])
CL Item
other (3)
C0205394 (UMLS CUI [1,1])
specify reason
Item
If other, please specify
text
C0205394 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
Dose administered
Item
Dose administered
float
C2348343 (UMLS CUI [1,1])
End 5-FU date
Item
End of 5-FU chemotherapy (date)
date
C0806020 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
End 5-FU time
Item
End of 5-FU chemotherapy (time)
time
C1522314 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Item Group
Calcium folinate and Granisetron treatment
C0061863 (UMLS CUI [1,1])
C0023413 (UMLS CUI [2,1])
Modification Calcium folinate
Item
Modification of planned Calcium folinate treatment?
boolean
C1299575 (UMLS CUI [1,1])
C0023413 (UMLS CUI [1,2])
Item
Reason for Calcium folinate dose modification
text
C0392360 (UMLS CUI [1,1])
Code List
Reason for Calcium folinate dose modification
CL Item
toxicity (1)
C0013221 (UMLS CUI [1,1])
CL Item
allergy (2)
C0013182 (UMLS CUI [1,1])
CL Item
other (3)
C0205394 (UMLS CUI [1,1])
specify reason
Item
If other, please specify
text
C0205394 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
Modification Granisetron
Item
Modification of planned Granisetron treatment?
boolean
C1299575 (UMLS CUI [1,1])
C0061863 (UMLS CUI [1,2])
specify discrepancy
Item
If yes, please specify discrepancy
text
C1521902 (UMLS CUI [1,1])
C3840684) (UMLS CUI [1,2])
Item Group
Surgery
C0543467 (UMLS CUI [1,1])
Date of surgery
Item
Date of surgery
date
C0011008 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
Item Group
Intraoperative re-evaluation of resectability
C0456904 (UMLS CUI [1,1])
C0681840 (UMLS CUI [1,2])
C5396338 (UMLS CUI [1,3])
Item
Result of intraoperative re-evaluation of resectability
text
C1274040 (UMLS CUI [1,1])
C0456904 (UMLS CUI [1,2])
C0681840 (UMLS CUI [1,3])
C5396338 (UMLS CUI [1,4])
Code List
Result of intraoperative re-evaluation of resectability
CL Item
intraoperative eligibility (1)
C0013893 (UMLS CUI [1,1])
C0456904 (UMLS CUI [1,2])
CL Item
violation of intraoperative eligibility (2)
C1709750 (UMLS CUI [1,1])
C0456904 (UMLS CUI [1,2])
C0013893 (UMLS CUI [1,3])
Exclusion of liver metastasis
Item
Exclusion of liver metastasis
boolean
C2828389 (UMLS CUI [1,1])
C0494165 (UMLS CUI [1,2])
Exclusion of peritoneal carcinomatosis
Item
Exclusion of peritoneal carcinomatosis
boolean
C2828389 (UMLS CUI [1,1])
C0346990 (UMLS CUI [1,2])
Exclusion of superior mesenteric / hepatic artery encasement
Item
Exclusion of superior mesenteric / hepatic artery encasement
boolean
C2828389 (UMLS CUI [1,1])
C4524504 (UMLS CUI [1,2])
C0019145 (UMLS CUI [1,3])
C0162861 (UMLS CUI [1,4])
Item Group
Tumor location (pancreas)
C2063875 (UMLS CUI [1,1])
uncinate process
Item
uncinate process
boolean
C0227580 (UMLS CUI [1,1])
head
Item
head
boolean
C0227579 (UMLS CUI [1,1])
body
Item
body
boolean
C0227582 (UMLS CUI [1,1])
tail
Item
tail
boolean
C0227590 (UMLS CUI [1,1])
Item Group
Surgery Details
C5204320 (UMLS CUI [1,1])
Start
Item
Start skin incision (time)
time
C0191279 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
End
Item
End of surgery (time)
time
C1522314 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
Item
Performed surgical intervention
text
C4035998 (UMLS CUI [1,1])
Code List
Performed surgical intervention
CL Item
partial pancreaticoduodenectomy (1)
C0728938 (UMLS CUI [1,1])
C0085162 (UMLS CUI [1,2])
CL Item
total pancreaticoduodenectomy (2)
C2945589 (UMLS CUI [1,1])
CL Item
pancreatic left resection (3)
C0400472 (UMLS CUI [1,1])
CL Item
other (4)
C0205394 (UMLS CUI [1,1])
specify surgical intervention
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Item Group
Additional resections
C1524062 (UMLS CUI [1,1])
C0015252 (UMLS CUI [1,2])
Vascular resections
Item
Vascular (venous) resections and reconstructions
boolean
C0189617 (UMLS CUI [1,1])
Item Group
Vascular (venous) resections and reconstructions
C0189617 (UMLS CUI [1,1])
portal venous resection
Item
portal venous resection
boolean
C0226727 (UMLS CUI [1,1])
C00152526 (UMLS CUI [1,2])
VMS resection
Item
VMS resection
boolean
C0226742 (UMLS CUI [1,1])
C0015252 (UMLS CUI [1,2])
other
Item
other
boolean
C0205394 (UMLS CUI [1,1])
specify vascular resections
Item
If other vascular resection, please specify
text
C1521902 (UMLS CUI [1,1])
Item Group
Additional resections
C1524062 (UMLS CUI [1,1])
C0015252 (UMLS CUI [1,2])
Additional resections
Item
Additional resections
boolean
C1706712 (UMLS CUI [1,1])
C0015252 (UMLS CUI [1,2])
Item Group
If yes, please specify additional resections
C1521902 (UMLS CUI [1,1])
lymphadenectomy
Item
lymphadenectomy
boolean
C0024203 (UMLS CUI [1,1])
extrapancreatic resections
Item
extrapancreatic resections
boolean
C0015252 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0030274 (UMLS CUI [1,3])
other
Item
other
boolean
C0205394 (UMLS CUI [1,1])
specify extrapancreatic resection
Item
If extrapancreatic resection, please specify
text
C1521902 (UMLS CUI [1,1])
specify other
Item
If other, please specify
text
C1521902 (UMLS CUI [1,1])
Item Group
Blood loss and Transfusion
C3163616 (UMLS CUI [1,1])
C0005841 (UMLS CUI [1,2])
Intraoperative blood loss
Item
Intraoperative blood loss (as estimated from the anesthesia protocol)
boolean
C5208110 (UMLS CUI [1,1])
specify blood loss
Item
If yes, please specify
float
C1521902 (UMLS CUI [1,1])
Blood transfusion
Item
Blood transfusion
boolean
C0005841 (UMLS CUI [1,1])
Item Group
Type of blood transfusion
C5420007 (UMLS CUI [1,1])
red blood cell concentrates
Item
red blood cell concentrates
boolean
C0086252 (UMLS CUI [1,1])
Volume red blood cell concentrates
Item
Volume of red blood cell concentrates
float
C0086252 (UMLS CUI [1,1])
C1264726 (UMLS CUI [1,2])
fresh frozen plasma (FFP)
Item
fresh frozen plasma (FFP)
boolean
C1293883 (UMLS CUI [1,1])
Volume FFPs
Item
Volume of fresh frozen plasma (FFP)
float
C1293883 (UMLS CUI [1,1])
C1264726 (UMLS CUI [1,2])
thrombocyte concentrates
Item
thrombocyte concentrates
boolean
C1293886 (UMLS CUI [1,1])
Volume thrombocyte concentrates
Item
Volume of thrombocyte concentrates
float
C1293886 (UMLS CUI [1,1])
C1264726 (UMLS CUI [1,2])
Item Group
Translational Studies
C1519620 (UMLS CUI [1,1])
Blood sample
Item
Blood sample taken (portal vein and peripheral vein)
boolean
C1277698 (UMLS CUI [1,1])
C2324289 (UMLS CUI [1,2])
C5401001 (UMLS CUI [1,3])
Bone marrow
Item
Bone marrow sample taken
boolean
C0005954 (UMLS CUI [1,1])
Tumor tissue
Item
Tumor tissue sample taken
boolean
C0475358 (UMLS CUI [1,1])
Item Group
Concomitant Medication
C2347852 (UMLS CUI [1,1])
changes in Concomitant Medication
Item
Any changes in Concomitant Medication (since last visit)?
boolean
C3872643 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
Item Group
If yes, please fill out eForm 'Concomitant Medication'
C3273494 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Item Group
Adverse Events
C0877248 (UMLS CUI [1,1])
Adverse Events occurred
Item
Any Adverse Events occurred since last visit?
boolean
C3872643 (UMLS CUI [1,1])
Item Group
If yes, please fill out eForm 'Adverse Events'
C0877248 (UMLS CUI [1,1])
C3273494 (UMLS CUI [1,2])
Item Group
Protocol violations
C1709750 (UMLS CUI [1,1])
protocol violations occurred
Item
Any protocol violations occurred since last visit?
boolean
C3872643 (UMLS CUI [1,1])
Item Group
If yes, please fill out eForm 'Protocol Violation'
C3273494 (UMLS CUI [1,1])

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