ID

43691

Beskrivning

Phase Ⅲ Randomized Trial in Postoperative Hepatocellular Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00149565

Länk

https://clinicaltrials.gov/show/NCT00149565

Nyckelord

Versioner (2)
  1. 2016-02-24 2016-02-24 -
  2. 2021-09-20 2021-09-20 -
Uppladdad den

20 september 2021

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT00149565

Engelsk

Eligibility Hepatocellular Carcinoma NCT00149565

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
1. histologically proven hepatocellular carcinoma.
Beskrivning

hepatocellular carcinoma

Datatyp

boolean

Alias
UMLS CUI [1]
C2239176
2. hcc underwent curative resection within 6 weeks before registration.
Beskrivning

surgery

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
3. grossly, the resection margin should be > 1 cm.
Beskrivning

resection margin

Datatyp

boolean

Alias
UMLS CUI [1]
C0229985
4. patients must be younger than 70 year-old.
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
5. patients must have a performance status of ecog score < 2.
Beskrivning

ecog

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
6. patients must have adequate liver reservation and adequate hemogram.
Beskrivning

liver function and hemogram

Datatyp

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0200631
7. pugh-child‘s score < 7.
Beskrivning

pugh-child score

Datatyp

boolean

Alias
UMLS CUI [1]
C4050412
8. the serum total bilirubin level are < 2 mg/dl.
Beskrivning

bilirubin

Datatyp

boolean

Alias
UMLS CUI [1]
C1278039
9. the prothrombin times are < 3 sec above normal control.
Beskrivning

prothrombin time

Datatyp

boolean

Alias
UMLS CUI [1]
C0033707
10. the platelet are > 10 x 104 / mm3.
Beskrivning

platelets

Datatyp

boolean

Alias
UMLS CUI [1]
C0005821
11. the wbc are > 3,000 / mm3.
Beskrivning

wbc

Datatyp

boolean

Alias
UMLS CUI [1]
C0023508
12. patient must have serum creatinine < 1.5 mg/dl
Beskrivning

creatinine

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
13. cardiac function with nyha classification < grade ii
Beskrivning

nyha

Datatyp

boolean

Alias
UMLS CUI [1]
C1275491
14. known hbv or hcv status.
Beskrivning

hbv or hcv

Datatyp

boolean

Alias
UMLS CUI [1]
C0019163
UMLS CUI [2]
C0019196
15. signed informed consent.
Beskrivning

informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
exclusion criteria:
Beskrivning

ID.16

Datatyp

boolean

1. patients who have non-curative resection are not eligible.
Beskrivning

surgery

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
2. resected hccs with histologically positive margins are not eligible.
Beskrivning

resection margins

Datatyp

boolean

Alias
UMLS CUI [1]
C0229985
3. hccs with radiological evidence of portal vein thrombus are not eligible.
Beskrivning

portal vein thrombus

Datatyp

boolean

Alias
UMLS CUI [1]
C2239176
UMLS CUI [2,1]
C0087086
UMLS CUI [2,2]
C0032718
4. patients with other systemic diseases which required concurrent usage of glucocorticosteroid or immunosuppressant agent(s) are not eligible.
Beskrivning

steroids or immunosuppressant agents

Datatyp

boolean

Alias
UMLS CUI [1]
C0038317
UMLS CUI [2]
C0021081
5. patients with advanced second primary malignancy are not eligible.
Beskrivning

malignancies

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
6. patients with pregnacy or breast-feeding are not eligible.
Beskrivning

pregnant or breast-feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
7. patients with severe cardiopulmonary diseases are not eligible.
Beskrivning

cardiopulmonary disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
8. patients with clinically significant psychiatric disorder are not eligible.
Beskrivning

psychiatric disorder

Datatyp

boolean

Alias
UMLS CUI [1]
C0004936
9. patients who had antineoplastic chemotherapeutic or immuno-therapeutic drugs or corticosteroids within 6 weeks of commencing the protocol are not eligible.
Beskrivning

chemotherapy, immuno-therapeutic drugs or steroids within 6 weeks

Datatyp

boolean

Alias
UMLS CUI [1]
C3665472
UMLS CUI [2]
C0876248
UMLS CUI [3]
C0007222
Tillbaka till toppen

Similar models

Eligibility Hepatocellular Carcinoma NCT00149565

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
hepatocellular carcinoma
Item
1. histologically proven hepatocellular carcinoma.
boolean
C2239176 (UMLS CUI [1])
surgery
Item
2. hcc underwent curative resection within 6 weeks before registration.
boolean
C0543467 (UMLS CUI [1])
resection margin
Item
3. grossly, the resection margin should be > 1 cm.
boolean
C0229985 (UMLS CUI [1])
Age
Item
4. patients must be younger than 70 year-old.
boolean
C0001779 (UMLS CUI [1])
ecog
Item
5. patients must have a performance status of ecog score < 2.
boolean
C1520224 (UMLS CUI [1])
liver function and hemogram
Item
6. patients must have adequate liver reservation and adequate hemogram.
boolean
C0232741 (UMLS CUI [1])
C0200631 (UMLS CUI [2])
pugh-child score
Item
7. pugh-child‘s score < 7.
boolean
C4050412 (UMLS CUI [1])
bilirubin
Item
8. the serum total bilirubin level are < 2 mg/dl.
boolean
C1278039 (UMLS CUI [1])
prothrombin time
Item
9. the prothrombin times are < 3 sec above normal control.
boolean
C0033707 (UMLS CUI [1])
platelets
Item
10. the platelet are > 10 x 104 / mm3.
boolean
C0005821 (UMLS CUI [1])
wbc
Item
11. the wbc are > 3,000 / mm3.
boolean
C0023508 (UMLS CUI [1])
creatinine
Item
12. patient must have serum creatinine < 1.5 mg/dl
boolean
C0201976 (UMLS CUI [1])
nyha
Item
13. cardiac function with nyha classification < grade ii
boolean
C1275491 (UMLS CUI [1])
hbv or hcv
Item
14. known hbv or hcv status.
boolean
C0019163 (UMLS CUI [1])
C0019196 (UMLS CUI [2])
informed consent
Item
15. signed informed consent.
boolean
C0021430 (UMLS CUI [1])
ID.16
Item
exclusion criteria:
boolean
surgery
Item
1. patients who have non-curative resection are not eligible.
boolean
C0543467 (UMLS CUI [1])
resection margins
Item
2. resected hccs with histologically positive margins are not eligible.
boolean
C0229985 (UMLS CUI [1])
portal vein thrombus
Item
3. hccs with radiological evidence of portal vein thrombus are not eligible.
boolean
C2239176 (UMLS CUI [1])
C0087086 (UMLS CUI [2,1])
C0032718 (UMLS CUI [2,2])
steroids or immunosuppressant agents
Item
4. patients with other systemic diseases which required concurrent usage of glucocorticosteroid or immunosuppressant agent(s) are not eligible.
boolean
C0038317 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
malignancies
Item
5. patients with advanced second primary malignancy are not eligible.
boolean
C0006826 (UMLS CUI [1])
pregnant or breast-feeding
Item
6. patients with pregnacy or breast-feeding are not eligible.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
cardiopulmonary disease
Item
7. patients with severe cardiopulmonary diseases are not eligible.
boolean
C0009488 (UMLS CUI [1])
psychiatric disorder
Item
8. patients with clinically significant psychiatric disorder are not eligible.
boolean
C0004936 (UMLS CUI [1])
chemotherapy, immuno-therapeutic drugs or steroids within 6 weeks
Item
9. patients who had antineoplastic chemotherapeutic or immuno-therapeutic drugs or corticosteroids within 6 weeks of commencing the protocol are not eligible.
boolean
C3665472 (UMLS CUI [1])
C0876248 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
Tillbaka till toppen 

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