ID

31334

Beschrijving

Green Tea Intake for the Maintenance of Complete Remission in Women With Advanced Ovarian Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00721890

Link

https://clinicaltrials.gov/show/NCT00721890

Trefwoorden

Versies (1)
  1. 14-08-18 14-08-18 -
Houder van rechten

See clinicaltrials.gov

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14 augustus 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Ovarian Carcinoma NCT00721890

Engels

Eligibility Ovarian Carcinoma NCT00721890

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with ovarian serous carcinoma figo stage iii or iv
Beschrijving

Ovarian Serous Carcinoma FIGO Stage

Datatype

boolean

Alias
UMLS CUI [1,1]
C1335177
UMLS CUI [1,2]
C0450454
patients showing complete response after oncological surgery and chemotherapy (paclitaxel-carboplatin, minimum 5 cycles, maximum 8 cycles), complete response being defined as 1) a negative complete physical examination 2) serum ca-125 levels inferior to 35 u/ml 3) no evidence of diseased assessed by abdomino-perineal ct-scan
Beschrijving

In complete remission Post Operative Surgical Procedures | In complete remission Post Chemotherapy | carboplatin/paclitaxel | Cycle Quantity Minimum | Cycle Quantity Maximum | Complete physical examination Negative | CA 125 measurement | Disease Free of CT of abdomen | Disease Free of Perineum CT scan

Datatype

boolean

Alias
UMLS CUI [1,1]
C0677874
UMLS CUI [1,2]
C0687676
UMLS CUI [1,3]
C0543467
UMLS CUI [2,1]
C0677874
UMLS CUI [2,2]
C0687676
UMLS CUI [2,3]
C0392920
UMLS CUI [3]
C0281297
UMLS CUI [4,1]
C1302181
UMLS CUI [4,2]
C1265611
UMLS CUI [4,3]
C1524031
UMLS CUI [5,1]
C1302181
UMLS CUI [5,2]
C1265611
UMLS CUI [5,3]
C0806909
UMLS CUI [6,1]
C0436120
UMLS CUI [6,2]
C1513916
UMLS CUI [7]
C0201549
UMLS CUI [8,1]
C0012634
UMLS CUI [8,2]
C0332296
UMLS CUI [8,3]
C0412620
UMLS CUI [9,1]
C0012634
UMLS CUI [9,2]
C0332296
UMLS CUI [9,3]
C0031066
UMLS CUI [9,4]
C0040405
patients refraining from drinking tea other than provided by the study
Beschrijving

Avoidance Drinking Tea | Exception Study Protocol Provided

Datatype

boolean

Alias
UMLS CUI [1,1]
C0870186
UMLS CUI [1,2]
C0684271
UMLS CUI [1,3]
C0039400
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C2348563
UMLS CUI [2,3]
C1999230
patients who may absorb liquids orally
Beschrijving

Ability Absorption Liquids Orally

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C0237442
UMLS CUI [1,3]
C0302908
UMLS CUI [1,4]
C0442027
patients without any other malignancy (except for non-melanoma skin cancer)
Beschrijving

Cancer Other Absent | Exception Skin carcinoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C1707251
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
patients not involved in an other study
Beschrijving

Absence Involvement with Clinical Trial Other

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C0008976
UMLS CUI [1,4]
C0205394
patients who signed up informed consent form.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
exclusion criteria are implicit from inclusion criteria.
Beschrijving

Exclusion Criteria Relationship Inclusion criteria

Datatype

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0439849
UMLS CUI [1,3]
C1512693
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Similar models

Eligibility Ovarian Carcinoma NCT00721890

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Ovarian Serous Carcinoma FIGO Stage
Item
patients with ovarian serous carcinoma figo stage iii or iv
boolean
C1335177 (UMLS CUI [1,1])
C0450454 (UMLS CUI [1,2])
In complete remission Post Operative Surgical Procedures | In complete remission Post Chemotherapy | carboplatin/paclitaxel | Cycle Quantity Minimum | Cycle Quantity Maximum | Complete physical examination Negative | CA 125 measurement | Disease Free of CT of abdomen | Disease Free of Perineum CT scan
Item
patients showing complete response after oncological surgery and chemotherapy (paclitaxel-carboplatin, minimum 5 cycles, maximum 8 cycles), complete response being defined as 1) a negative complete physical examination 2) serum ca-125 levels inferior to 35 u/ml 3) no evidence of diseased assessed by abdomino-perineal ct-scan
boolean
C0677874 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
C0677874 (UMLS CUI [2,1])
C0687676 (UMLS CUI [2,2])
C0392920 (UMLS CUI [2,3])
C0281297 (UMLS CUI [3])
C1302181 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C1524031 (UMLS CUI [4,3])
C1302181 (UMLS CUI [5,1])
C1265611 (UMLS CUI [5,2])
C0806909 (UMLS CUI [5,3])
C0436120 (UMLS CUI [6,1])
C1513916 (UMLS CUI [6,2])
C0201549 (UMLS CUI [7])
C0012634 (UMLS CUI [8,1])
C0332296 (UMLS CUI [8,2])
C0412620 (UMLS CUI [8,3])
C0012634 (UMLS CUI [9,1])
C0332296 (UMLS CUI [9,2])
C0031066 (UMLS CUI [9,3])
C0040405 (UMLS CUI [9,4])
Avoidance Drinking Tea | Exception Study Protocol Provided
Item
patients refraining from drinking tea other than provided by the study
boolean
C0870186 (UMLS CUI [1,1])
C0684271 (UMLS CUI [1,2])
C0039400 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C1999230 (UMLS CUI [2,3])
Ability Absorption Liquids Orally
Item
patients who may absorb liquids orally
boolean
C0085732 (UMLS CUI [1,1])
C0237442 (UMLS CUI [1,2])
C0302908 (UMLS CUI [1,3])
C0442027 (UMLS CUI [1,4])
Cancer Other Absent | Exception Skin carcinoma
Item
patients without any other malignancy (except for non-melanoma skin cancer)
boolean
C1707251 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
Absence Involvement with Clinical Trial Other
Item
patients not involved in an other study
boolean
C0332197 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
Informed Consent
Item
patients who signed up informed consent form.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Exclusion Criteria Relationship Inclusion criteria
Item
exclusion criteria are implicit from inclusion criteria.
boolean
C0680251 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,3])
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