ID
37619
Description
Study ID: 104864/612 Clinical Study ID: 104864/612 Study Title: A Prospective, Open Label Phase II Study to Evaluate the Efficacy and Safety of Topotecan (HycamtinTM) in Combination with Carboplatin as First-line Chemotherapy in Patients with Ovarian Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan Trade Name: HycamtinTM Study Indication: Ovarian Cancer
Mots-clés
Versions (1)
- 11/08/2019 11/08/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
11 août 2019
DOI
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Licence
Creative Commons BY-NC 3.0
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Topotecan (HycamtinTM) with Carboplatin as First-Line Chemotherapy in Patients with Ovarian Cancer; 104864/612
Eligibility Determination
- StudyEvent: ODM
Description
Inclusion Criteria
Alias
- UMLS CUI-1
- C1512693
Description
Epithelial Ovarian Cancer, FIGO stage
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0677886
- UMLS CUI [1,2]
- C0450454
Description
Prior Chemotherapy; prior radiation therapy
Type de données
boolean
Alias
- UMLS CUI [1]
- C1514457
- UMLS CUI [2]
- C0279134
Description
Age
Type de données
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
ECOG performance status, Karnofsky Performance status
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1520224
- UMLS CUI [1,2]
- C0206065
Description
Life Expectancy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0023671
Description
Residual Tumor
Type de données
boolean
Alias
- UMLS CUI [1]
- C0543478
Description
Hemotologic function; Renal function; Liver function
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0221130
- UMLS CUI [1,2]
- C0232804
- UMLS CUI [1,3]
- C0232741
Description
Informed Consent
Type de données
boolean
Alias
- UMLS CUI [1]
- C0021430
Description
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Description
Epithelioma; Mucinous cystic tumor of borderline malignancy
Type de données
boolean
Alias
- UMLS CUI [1]
- C1368683
- UMLS CUI [2]
- C0334365
Description
Prior Chemotherapy; prior radiation therapy
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1514457
- UMLS CUI [1,2]
- C0279134
Description
Residual Tumor
Type de données
boolean
Alias
- UMLS CUI [1]
- C0543478
Description
Communicable Disease; Disease
Type de données
boolean
Alias
- UMLS CUI [1]
- C000945
- UMLS CUI [2]
- C0012634
Description
Dementia; Abnormal mental state
Type de données
boolean
Alias
- UMLS CUI [1]
- C0497327
- UMLS CUI [2]
- C0278061
Description
Experimental drug, Hypersensitivity
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0020517
Description
Other medical condition,at risk; Therapeutic procedure, at risk
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C3843040
- UMLS CUI [1,2]
- C1444641
- UMLS CUI [2,1]
- C0087111
- UMLS CUI [2,2]
- C1444641
Description
Malignant Neoplasms
Type de données
boolean
Alias
- UMLS CUI [1]
- C0006826
Description
Chemotherapy, Simultaneous; Hormone therapy, Simultaneous; Therapeutic radiology procedure, Simultaneous
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C3665472
- UMLS CUI [1,2]
- C0521115
- UMLS CUI [2,1]
- C0279025
- UMLS CUI [2,2]
- C0521115
- UMLS CUI [3,1]
- C1522449
- UMLS CUI [3,2]
- C0521115
Similar models
Eligibility Determination
- StudyEvent: ODM
C0450454 (UMLS CUI [1,2])
C0279134 (UMLS CUI [2])
C0206065 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,2])
C0232741 (UMLS CUI [1,3])
C0334365 (UMLS CUI [2])
C0279134 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2])
C0278061 (UMLS CUI [2])
C0020517 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C1444641 (UMLS CUI [2,2])
C0521115 (UMLS CUI [1,2])
C0279025 (UMLS CUI [2,1])
C0521115 (UMLS CUI [2,2])
C1522449 (UMLS CUI [3,1])
C0521115 (UMLS CUI [3,2])