Breast Cancer Clinical Trial
— WiZenOfficial title:
Wirksamkeit Der Versorgung in Onkologischen Zentren
NCT number | NCT04334239 |
Other study ID # | 01VSF17020 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | May 1, 2017 |
Est. completion date | August 31, 2021 |
Verified date | August 2022 |
Source | Technische Universität Dresden |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Assessment of the effectiveness of care in certified cancer centres for eight cancer entities via a retrospective cohort study based on secondary data from statutory health insurance funds and population-based clinical cancer registries.
Status | Completed |
Enrollment | 670000 |
Est. completion date | August 31, 2021 |
Est. primary completion date | May 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - first hospitalization due to diagnosis of colorectal cancer, pancreatic cancer, breast cancer, gynecologic tumors, lung cancer, prostate cancer, head and neck tumors, or neuro-oncological tumors 2009-2017 [WIdO] - hospitalization due to primary diagnosis of colorectal cancer, pancreatic cancer, breast cancer, gynecologic tumors, lung cancer, prostate cancer, head and neck tumors, or neuro-oncological tumors 2006-2017 [CCR] Exclusion Criteria: - prevalent diagnosis of colorectal cancer, pancreatic cancer, breast cancer, gynecologic tumors, lung cancer, prostate cancer, head and neck tumors, or neuro-oncological tumors 2006-2017 - exception: outpatient cancer diagnosis up to 12 months prior to first hospitalization is not regarded as prevalent |
Country | Name | City | State |
---|---|---|---|
Germany | Technische Universität Dresden | Dresden | Sachsen |
Lead Sponsor | Collaborator |
---|---|
Technische Universität Dresden | Arbeitsgemeinschaft Deutscher Tumorzenten e.V., ADT, Tumorzentrum Regensburg, Institut für Qualitätssicherung und Versorgungsforschung, Universität Regensburg, Wissenschaftliches Institut der AOK (WIdO) |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Overall survival | Survival after first hospitalization due to cancer | first hospitalization (starting from 01/01/2009 [WIdO] or 01/01/2006 [CCR]), up to 31/12/2017 | |
Primary | 1- and 5-year survival | 1- and 5-year survival after first hospitalization due to cancer | first hospitalization (starting from 01/01/2009 [WIdO] or 01/01/2006 [CCR]) with 1 or 5-year follow-up, respectively | |
Primary | 30-day mortality | 30-day mortality after first hospitalization due to cancer | first hospitalization (starting from 01/01/2009 [WIdO] or 01/01/2006 [CCR]) with 30 days follow-up | |
Secondary | 2-, 3-, 4-year survival | 2-, 3-, 4-year survival after first hospitalization due to cancer | first hospitalization (starting from 01/01/2009 [WIdO] or 01/01/2006 [CCR]) with 2,3, or 4-year follow-up, respectively | |
Secondary | Recurrence-free survival | Recurrence-free survival after cancer diagnosis | cancer diagnosis (starting from 01/01/2009 [WIdO] or 01/01/2006 [CCR]), up to 31/12/2017 | |
Secondary | Cumulative recurrence rate | Cumulative recurrence rate after cancer diagnosis | cancer diagnosis (starting from 01/01/2009 [WIdO] or 01/01/2006 [CCR]), up to 31/12/2017 | |
Secondary | Complications due to surgery | Complications due to cancer surgery | date of initial cancer surgery with entity-specific follow-up | |
Secondary | Successive resection | Second resection due to cancer | second resection within three months of initial cancer surgery | |
Secondary | Entity-specific outcomes defined by clinical experts | Fractions of entity-specific surgery techniques
For head-neck-tumours: aspiration pneumonia due to swallowing dysfunctions |
2009-2017 [CCR] or 2006-2017 [WIdO] | |
Secondary | Fraction of patients | Fraction of patients in certified centres and in non-certified hospitals over time | 2009-2017 | |
Secondary | Regional differences | Differences across outcomes in different counties or federal states | 2009-2017 | |
Secondary | Differences in patient characteristics | Differences in demographic characteristics, disease severity and risk factors across certified centres/non-certified hospitals | 2009-2017 [CCR] or 2006-2017 [WIdO] | |
Secondary | Pathways of treatment | Patient's treatment pathways among general practitioners, specialists, and hospitals w.r.t. certification | 2009-2017 | |
Secondary | Severity Levels in insurance data | Deduction of cancer severity levels through linkage of health insurance and cancer registry data | 2009-2017 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04681911 -
Inetetamab Combined With Pyrotinib and Chemotherapy in the Treatment of HER2 Positive Metastatic Breast Cancer
|
Phase 2 | |
Terminated |
NCT04066790 -
Pyrotinib or Trastuzumab Plus Nab-paclitaxel as Neoadjuvant Therapy in HER2-positive Breast Cancer
|
Phase 2 | |
Completed |
NCT04890327 -
Web-based Family History Tool
|
N/A | |
Completed |
NCT03591848 -
Pilot Study of a Web-based Decision Aid for Young Women With Breast Cancer, During the Proposal for Preservation of Fertility
|
N/A | |
Recruiting |
NCT03954197 -
Evaluation of Priming Before in Vitro Maturation for Fertility Preservation in Breast Cancer Patients
|
N/A | |
Terminated |
NCT02202746 -
A Study to Assess the Safety and Efficacy of the VEGFR-FGFR-PDGFR Inhibitor, Lucitanib, Given to Patients With Metastatic Breast Cancer
|
Phase 2 | |
Active, not recruiting |
NCT01472094 -
The Hurria Older PatiEnts (HOPE) With Breast Cancer Study
|
||
Withdrawn |
NCT06057636 -
Hypnosis for Pain in Black Women With Advanced Breast Cancer: A Feasibility Study
|
N/A | |
Completed |
NCT06049446 -
Combining CEM and Magnetic Seed Localization of Non-Palpable Breast Tumors
|
||
Recruiting |
NCT05560334 -
A Single-Arm, Open, Exploratory Clinical Study of Pemigatinib in the Treatment of HER2-negative Advanced Breast Cancer Patients With FGFR Alterations
|
Phase 2 | |
Active, not recruiting |
NCT05501769 -
ARV-471 in Combination With Everolimus for the Treatment of Advanced or Metastatic ER+, HER2- Breast Cancer
|
Phase 1 | |
Recruiting |
NCT04631835 -
Phase I Study of the HS-10352 in Patients With Advanced Breast Cancer
|
Phase 1 | |
Completed |
NCT04307407 -
Exercise in Breast Cancer Survivors
|
N/A | |
Recruiting |
NCT03544762 -
Correlation of 16α-[18F]Fluoro-17β-estradiol PET Imaging With ESR1 Mutation
|
Phase 3 | |
Terminated |
NCT02482389 -
Study of Preoperative Boost Radiotherapy
|
N/A | |
Enrolling by invitation |
NCT00068003 -
Harvesting Cells for Experimental Cancer Treatments
|
||
Completed |
NCT00226967 -
Stress, Diurnal Cortisol, and Breast Cancer Survival
|
||
Recruiting |
NCT06006390 -
CEA Targeting Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of CEA Positive Advanced Solid Tumors
|
Phase 1/Phase 2 | |
Recruiting |
NCT06037954 -
A Study of Mental Health Care in People With Cancer
|
N/A | |
Recruiting |
NCT06019325 -
Rhomboid Intercostal Plane Block on Chronic Pain Incidence and Acute Pain Scores After Mastectomy
|
N/A |