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Información:
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ID
15156
Descripción
Comprehensive Patient Questionnaires in Predicting Complications in Older Patients With Gynecologic Cancer Undergoing Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT02315469
Link
https://clinicaltrials.gov/show/NCT02315469
Palabras clave
Versiones (2)
- 19/5/16 19/5/16 -
- 20/9/21 20/9/21 -
Subido en
19 de mayo de 2016
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Fallopian Tube Carcinoma NCT02315469
Eligibility Fallopian Tube Carcinoma NCT02315469
- StudyEvent: Eligibility
Similar models
Eligibility Fallopian Tube Carcinoma NCT02315469
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Ovarian Carcinoma | Fallopian Tube Neoplasms | Primary Peritoneal Carcinoma | Papillary carcinoma of uterus Advanced phase | performance status
Item
patients with suspected ovarian, fallopian tube, primary peritoneal carcinomas or advanced stage papillary serous uterine carcinoma irrespective of performance status; this clinical determination is made by the treating physician
boolean
C0029925 (UMLS CUI [1])
C0015558 (UMLS CUI [2])
C1514428 (UMLS CUI [3])
C0279764 (UMLS CUI [4,1])
C0205179 (UMLS CUI [4,2])
C1518965 (UMLS CUI [5])
C0015558 (UMLS CUI [2])
C1514428 (UMLS CUI [3])
C0279764 (UMLS CUI [4,1])
C0205179 (UMLS CUI [4,2])
C1518965 (UMLS CUI [5])
Informed Consent
Item
patients must have signed an approved informed consent and authorization permitting release of personal health information
boolean
C0021430 (UMLS CUI [1])
Comprehension | Able to respond to communication by others | Study Protocol
Item
patients who can understand sufficiently to be able to respond to questions posed by the study instruments
boolean
C0162340 (UMLS CUI [1])
C0566155 (UMLS CUI [2])
C2348563 (UMLS CUI [3])
C0566155 (UMLS CUI [2])
C2348563 (UMLS CUI [3])
Patients | Caregiver | Consent | Response Questionnaires
Item
patients and/or caregiver (durable power of attorney) can give consent and caregiver can assist with the responses to questionnaire
boolean
C0030705 (UMLS CUI [1])
C0085537 (UMLS CUI [2])
C1511481 (UMLS CUI [3])
C2911692 (UMLS CUI [4,1])
C0034394 (UMLS CUI [4,2])
C0085537 (UMLS CUI [2])
C1511481 (UMLS CUI [3])
C2911692 (UMLS CUI [4,1])
C0034394 (UMLS CUI [4,2])
Age | Neoadjuvant Therapy Chemotherapy Regimen | Operative Surgical Procedures Interval | Cytoreduction Surgical Procedures
Item
note: it is the intent of this trial that all patients 70 years or older presenting to the participating physician/center be offered enrollment onto this study; eligible patients may enroll and subsequently receive neoadjuvant chemotherapy followed by interval surgery, primary cytoreductive surgery or no surgery at all
boolean
C0001779 (UMLS CUI [1])
C0600558 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0543467 (UMLS CUI [3,1])
C1272706 (UMLS CUI [3,2])
C3850079 (UMLS CUI [4])
C0600558 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0543467 (UMLS CUI [3,1])
C1272706 (UMLS CUI [3,2])
C3850079 (UMLS CUI [4])
Pathology Postoperative
Item
post-operative pathology will not exclude patients from this study
boolean
C0205469 (UMLS CUI [1,1])
C0231287 (UMLS CUI [1,2])
C0231287 (UMLS CUI [1,2])
Life circumstances Compliance behavior Limited
Item
patients whose circumstances at the time of study entry do not permit completion of the study or required follow-up
boolean
C0680082 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Minimally Invasive Surgical Procedures | Cytoreductive surgery | Ovarian Carcinoma | Fallopian Tube Neoplasms | Malignant tumor of peritoneum | Advanced phase
Item
patients who would have planned surgery performed by the minimally invasive technique; institutions which perform cytoreductive surgery via the minimally invasive technique should not participate in this study; the minimally invasive surgery (mis) technique is also not considered standard technique for primary cytoreductive surgery for advanced stage ovarian, fallopian tube or peritoneal cancers
boolean
C0282624 (UMLS CUI [1])
C1112438 (UMLS CUI [2])
C0029925 (UMLS CUI [3])
C0015558 (UMLS CUI [4])
C0153467 (UMLS CUI [5])
C0205179 (UMLS CUI [6])
C1112438 (UMLS CUI [2])
C0029925 (UMLS CUI [3])
C0015558 (UMLS CUI [4])
C0153467 (UMLS CUI [5])
C0205179 (UMLS CUI [6])
Chemotherapy Regimen | Malignant Neoplasms Gynecologic | Geriatric Assessment
Item
patients who receive chemotherapy treatment (for a gynecologic malignancy) prior to consideration of enrollment into this trial and taking the geriatric assessment will be excluded
boolean
C0392920 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C0205480 (UMLS CUI [2,2])
C0017463 (UMLS CUI [3])
C0006826 (UMLS CUI [2,1])
C0205480 (UMLS CUI [2,2])
C0017463 (UMLS CUI [3])
Uterine Cancer Preoperative | Endometrial biopsy
Item
patients who have a known pre-operative primary uterine cancer, confirmed by endometrial biopsy
boolean
C0153567 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C1510477 (UMLS CUI [2])
C0445204 (UMLS CUI [1,2])
C1510477 (UMLS CUI [2])