ID

28299

Beschrijving

Curcumin in Preventing Colorectal Cancer in Patients Undergoing Colorectal Endoscopy or Colorectal Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT00973869

Link

https://clinicaltrials.gov/show/NCT00973869

Trefwoorden

Versies (1)
  1. 02-01-18 02-01-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

2 januari 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00973869

Engels

Eligibility Colorectal Cancer NCT00973869

1 Formulieren  
Criteria
Beschrijving

Criteria

meets 1 of the following criteria:
Beschrijving

Criteria Fulfill

Datatype

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
has a positive fecal occult blood test found during a pilot colorectal cancer screening program
Beschrijving

Fecal occult blood positive Colorectal cancer screening

Datatype

boolean

Alias
UMLS CUI [1,1]
C0266813
UMLS CUI [1,2]
C0281185
awaiting diagnostic or surveillance colonoscopy
Beschrijving

Colonoscopy Expected | Colonoscopy Surveillance Expected

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009378
UMLS CUI [1,2]
C1517001
UMLS CUI [2,1]
C0009378
UMLS CUI [2,2]
C0220920
UMLS CUI [2,3]
C1517001
diagnosis of colorectal cancer
Beschrijving

Colorectal Carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0009402
patient characteristics:
Beschrijving

Client Characteristics

Datatype

boolean

Alias
UMLS CUI [1]
C0815172
able to return for follow-up tests
Beschrijving

Patient Available Follow-up Tests

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C3274571
UMLS CUI [1,4]
C0022885
fertile patients must use effective contraception
Beschrijving

Fertility Contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0700589
no discrete gastric or duodenal ulcer > 5 mm in the past year
Beschrijving

Exclusion Criteria | Gastric ulcer discrete Size | Duodenal Ulcer discrete Size

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0038358
UMLS CUI [2,2]
C0443299
UMLS CUI [2,3]
C0456389
UMLS CUI [3,1]
C0013295
UMLS CUI [3,2]
C0443299
UMLS CUI [3,3]
C0456389
patients with a history of helicobacter pylori-related peptic ulcer disease are eligible after successfully completing antibiotic treatment for helicobacter pylori
Beschrijving

Peptic Ulcer Helicobacter pylori Related | Antibiotic therapy Completed Helicobacter pylori

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030920
UMLS CUI [1,2]
C0079488
UMLS CUI [1,3]
C0439849
UMLS CUI [2,1]
C0338237
UMLS CUI [2,2]
C0205197
UMLS CUI [2,3]
C0079488
no significant medical or psychiatric problem, including significant renal, hepatic, or hematological dysfunction, that would make the patient a poor candidate for this study
Beschrijving

Exclusion Criteria | Medical Problem Study Subject Participation Status Poor | Psychiatric problem Study Subject Participation Status Poor | Renal dysfunction | Liver Dysfunction | Dysfunction Hematologic

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C1254481
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C2700379
UMLS CUI [3,1]
C1306597
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C2700379
UMLS CUI [4]
C3279454
UMLS CUI [5]
C0086565
UMLS CUI [6,1]
C3887504
UMLS CUI [6,2]
C0205488
prior concurrent therapy:
Beschrijving

Therapeutic procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
more than 3 months since prior investigational agents
Beschrijving

Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C0013230
no prior pelvic radiotherapy
Beschrijving

Exclusion | Radiotherapy to pelvis

Datatype

boolean

Alias
UMLS CUI [1]
C2828389
UMLS CUI [2]
C1536155
no other concurrent investigational agents
Beschrijving

Exclusion | Investigational New Drugs Other

Datatype

boolean

Alias
UMLS CUI [1]
C2828389
UMLS CUI [2,1]
C0013230
UMLS CUI [2,2]
C0205394
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Similar models

Eligibility Colorectal Cancer NCT00973869

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Criteria Fulfill
Item
meets 1 of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Fecal occult blood positive Colorectal cancer screening
Item
has a positive fecal occult blood test found during a pilot colorectal cancer screening program
boolean
C0266813 (UMLS CUI [1,1])
C0281185 (UMLS CUI [1,2])
Colonoscopy Expected | Colonoscopy Surveillance Expected
Item
awaiting diagnostic or surveillance colonoscopy
boolean
C0009378 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C0009378 (UMLS CUI [2,1])
C0220920 (UMLS CUI [2,2])
C1517001 (UMLS CUI [2,3])
Colorectal Carcinoma
Item
diagnosis of colorectal cancer
boolean
C0009402 (UMLS CUI [1])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Patient Available Follow-up Tests
Item
able to return for follow-up tests
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C0022885 (UMLS CUI [1,4])
Fertility Contraceptive methods
Item
fertile patients must use effective contraception
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Exclusion Criteria | Gastric ulcer discrete Size | Duodenal Ulcer discrete Size
Item
no discrete gastric or duodenal ulcer > 5 mm in the past year
boolean
C0680251 (UMLS CUI [1])
C0038358 (UMLS CUI [2,1])
C0443299 (UMLS CUI [2,2])
C0456389 (UMLS CUI [2,3])
C0013295 (UMLS CUI [3,1])
C0443299 (UMLS CUI [3,2])
C0456389 (UMLS CUI [3,3])
Peptic Ulcer Helicobacter pylori Related | Antibiotic therapy Completed Helicobacter pylori
Item
patients with a history of helicobacter pylori-related peptic ulcer disease are eligible after successfully completing antibiotic treatment for helicobacter pylori
boolean
C0030920 (UMLS CUI [1,1])
C0079488 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0338237 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0079488 (UMLS CUI [2,3])
Exclusion Criteria | Medical Problem Study Subject Participation Status Poor | Psychiatric problem Study Subject Participation Status Poor | Renal dysfunction | Liver Dysfunction | Dysfunction Hematologic
Item
no significant medical or psychiatric problem, including significant renal, hepatic, or hematological dysfunction, that would make the patient a poor candidate for this study
boolean
C0680251 (UMLS CUI [1])
C1254481 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C2700379 (UMLS CUI [2,3])
C1306597 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C2700379 (UMLS CUI [3,3])
C3279454 (UMLS CUI [4])
C0086565 (UMLS CUI [5])
C3887504 (UMLS CUI [6,1])
C0205488 (UMLS CUI [6,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Investigational New Drugs
Item
more than 3 months since prior investigational agents
boolean
C0013230 (UMLS CUI [1])
Exclusion | Radiotherapy to pelvis
Item
no prior pelvic radiotherapy
boolean
C2828389 (UMLS CUI [1])
C1536155 (UMLS CUI [2])
Exclusion | Investigational New Drugs Other
Item
no other concurrent investigational agents
boolean
C2828389 (UMLS CUI [1])
C0013230 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
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