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16 Zoekresultaten.

Non-Surgical Intervention GSK study Prostatic neoplasms NCT00883909

- 26-11-17 - 1 Formulier, 3 Itemgroepen, 12 Data-elementen, 1 Taal

Itemgroepen: Administrative data, Intervention non-surgical Prostate Cancer, Intervention non-surgical

Study ID: 103094 Clinical Study ID: ARI103094 Study Title: ARI103094-Follow-Up Study for REDUCE Study Subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00883909 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: dutasteride Trade Name: Zytefor,Zyfetor,Duagen,Avolve,Avodart,Avidart Study Indication: Neoplasms, Prostate

Concomitant Medications GSK study Prostatic neoplasms NCT00883909

- 26-11-17 - 1 Formulier, 3 Itemgroepen, 15 Data-elementen, 1 Taal

Itemgroepen: Administrative data, Concomitant Medications, Concomitant Medication

Study ID: 103094 Clinical Study ID: ARI103094 Study Title: ARI103094-Follow-Up Study for REDUCE Study Subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00883909 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: dutasteride Trade Name: Zytefor,Zyfetor,Duagen,Avolve,Avodart,Avidart Study Indication: Neoplasms, Prostate

Hypofractionated Radiotherapy in Prostate Cancer NCT01368055 - Eligibility Criteria

- 15-03-21 - 1 Formulier, 2 Itemgroepen, 10 Data-elementen, 1 Taal

Itemgroepen: Inclusion Criteria, Exclusion Criteria

Hypofractionated Proton Radiation Therapy for Low and Intermediate Risk Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01368055

HistoScanning-based Brachytherapy in Prostate Cancer NCT01409876 - Eligibility Criteria

- 22-05-19 - 1 Formulier, 2 Itemgroepen, 11 Data-elementen, 1 Taal

Itemgroepen: Inclusion Criteria, Exclusion Criteria

Phase II trial looking at the feasibility of HistoScanning-based dose-painting image-guided interstitial brachytherapy in non-metastatic prostate cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01409876

SABR in High Risk Prostate Cancer (SATURN) NCT01953055 - Eligibility Criteria

- 22-05-19 - 1 Formulier, 2 Itemgroepen, 10 Data-elementen, 1 Taal

Itemgroepen: Inclusion Criteria, Exclusion Criteria

Phase II Study of Stereotactic Ablative Radiotherapy Including Regional Lymph Node Irradiation for Patients With High Risk Prostate Cancer (SATURN); ODM derived from: https://clinicaltrials.gov/show/NCT01953055

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 11 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 11

- 24-05-17 - 1 Formulier, 22 Itemgroepen, 135 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 10 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 10

- 24-05-17 - 1 Formulier, 22 Itemgroepen, 135 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 9 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 9

- 24-05-17 - 1 Formulier, 22 Itemgroepen, 135 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 8 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 8

- 24-05-17 - 1 Formulier, 22 Itemgroepen, 135 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 7 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 7

- 24-05-17 - 1 Formulier, 22 Itemgroepen, 135 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 6 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 6

- 24-05-17 - 1 Formulier, 22 Itemgroepen, 139 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 4 - CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 4

- 24-05-17 - 1 Formulier, 23 Itemgroepen, 136 Data-elementen, 1 Taal

Itemgroepen: Visit Information, Vital Signs, Laboratory Tests Hematology, Laboratory Tests Biochemistry, Premedication, Investigational Product Administration - Prednisone, Investigational Product Administration - Cabazitaxel, Interruption - Cabazitaxel, Circulating free plasma DNA - Blood Sampling, Macroscopic Hematuria, Tumor Assessment - Target Lesion, Tumor Assessment - Non-target lesion, Tumor Assessment - New Lesion, Bone Scan, Tumor Markers, Cancer Pain Questionnaire, Disease Status, FACT P Questionnaire, FACT P Questionnaire - Physical Well-Being, FACT P Questionnaire - Social/ Family Well-Being, FACT P Questionnaire - Emotional Well-Being, FACT P Quesionnaire - Functional Well-Being, FACT P Questionnaire - Additional Concerns

Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi

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