ID
31614
Descripción
Consolidation Whole Abdominal Intensity-Modulated Radiation Therapy (IMRT) in Advanced Ovarian Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01180504 Sponsor: University Hospital Heidelberg Collaborator: Deutsche Krebshilfe e.V., Bonn (Germany) Information provided by: University Hospital Heidelberg Principal Investigator: Andreas Schneeweiss, MD Department of Gyneacology and Obstetrics, Unversity of Heidelberg Principal Investigator: Juergen Debus, MD, PhD Department of Radiation Oncology, University of Heidelberg
Link
https://clinicaltrials.gov/show/NCT01180504
Palabras clave
Versiones (1)
- 12/9/18 12/9/18 -
Titular de derechos de autor
Juergen Debus / Prof., M.D., PhD, Department of Radiation Oncology, University of Heidelberg
Subido en
12 de septiembre de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Eligibility Ovarian Cancer NCT01180504
Eligibility Ovarian Cancer NCT01180504
- StudyEvent: Eligibility
Descripción
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Descripción
stage figo i or ii
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0474956
Descripción
stage iii with postoperative gross residual tumor > 1cm
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0474956
- UMLS CUI [1,2]
- C0475286
Descripción
stage figo iv
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0474956
Descripción
Recurrence situation
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0034897
Descripción
delayed wound healing post laparotomy
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0151692
- UMLS CUI [1,2]
- C0023038
Descripción
Leucopenia <2000/ml before radiotherapy
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0023530
Descripción
Thrombocytopenia <75000/ml before radiotherapy
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0040034
Descripción
clinically active renal, hepatic, cardiac, metabolic, respiratory, coagulation or hematopoietic disease
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0022658
- UMLS CUI [2]
- C0023895
- UMLS CUI [3]
- C0018799
- UMLS CUI [4]
- C0025517
- UMLS CUI [5]
- C0035204
- UMLS CUI [6]
- C0005779
- UMLS CUI [7]
- C1292123
Descripción
status post pelvic or abdominal radiotherapy
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0231290
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [1,3]
- C0030797
- UMLS CUI [2,1]
- C0231290
- UMLS CUI [2,2]
- C1522449
- UMLS CUI [2,3]
- C0000726
Descripción
History of other cancer disease in the past 5 years exluding cervical cancer in situ, basal cell carcinoma, squamous cell carcinoma of the skin
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2735087
- UMLS CUI [2,1]
- C2828389
- UMLS CUI [2,2]
- C0851140
- UMLS CUI [3,1]
- C2828389
- UMLS CUI [3,2]
- C0007117
- UMLS CUI [4,1]
- C2828389
- UMLS CUI [4,2]
- C0553723
Descripción
Participation in another clinical trial
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2348568
Similar models
Eligibility Ovarian Cancer NCT01180504
- StudyEvent: Eligibility
C0029925 (UMLS CUI [1,2])
C0474956 (UMLS CUI [1,3])
C0449575 (UMLS CUI [2,1])
C0153579 (UMLS CUI [2,2])
C0474956 (UMLS CUI [2,3])
C0449575 (UMLS CUI [3,1])
C1514428 (UMLS CUI [3,2])
C0474956 (UMLS CUI [3,3])
C1706406 (UMLS CUI [1,2])
C0475440 (UMLS CUI [1,2])
C3536920 (UMLS CUI [1,2])
C0085533 (UMLS CUI [2,1])
C3541958 (UMLS CUI [2,2])
C0392920 (UMLS CUI [1,2])
C0475286 (UMLS CUI [1,2])
C0023038 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2])
C0018799 (UMLS CUI [3])
C0025517 (UMLS CUI [4])
C0035204 (UMLS CUI [5])
C0005779 (UMLS CUI [6])
C1292123 (UMLS CUI [7])
C1522449 (UMLS CUI [1,2])
C0030797 (UMLS CUI [1,3])
C0231290 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
C0000726 (UMLS CUI [2,3])
C2828389 (UMLS CUI [2,1])
C0851140 (UMLS CUI [2,2])
C2828389 (UMLS CUI [3,1])
C0007117 (UMLS CUI [3,2])
C2828389 (UMLS CUI [4,1])
C0553723 (UMLS CUI [4,2])