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])
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])