ID

28299

Description

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

Keywords

Versions (1)
  1. 1/2/18 1/2/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 2, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0
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.

Eligibility Colorectal Cancer NCT00973869

English

Eligibility Colorectal Cancer NCT00973869

1 forms  
Criteria
Description

Criteria

meets 1 of the following criteria:
Description

Criteria Fulfill

Data type

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
Description

Fecal occult blood positive Colorectal cancer screening

Data type

boolean

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

Colonoscopy Expected | Colonoscopy Surveillance Expected

Data type

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
Description

Colorectal Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0009402
patient characteristics:
Description

Client Characteristics

Data type

boolean

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

Patient Available Follow-up Tests

Data type

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
Description

Fertility Contraceptive methods

Data type

boolean

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

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

Data type

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
Description

Peptic Ulcer Helicobacter pylori Related | Antibiotic therapy Completed Helicobacter pylori

Data type

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
Description

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

Data type

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:
Description

Therapeutic procedure

Data type

boolean

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

Investigational New Drugs

Data type

boolean

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

Exclusion | Radiotherapy to pelvis

Data type

boolean

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

Exclusion | Investigational New Drugs Other

Data type

boolean

Alias
UMLS CUI [1]
C2828389
UMLS CUI [2,1]
C0013230
UMLS CUI [2,2]
C0205394
Back to the top of the page

Similar models

Eligibility Colorectal Cancer NCT00973869

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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