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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date August 2022
Source Technische Universität Dresden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

Cancer constitutes the second most frequent cause of death in Germany. To maintain a high quality of treatment, the national cancer plan aims at a unified certification of cancer centres. The project "Wirksamkeit der Versorgung in onkologischen Zentren" (WiZen) investigates effects of treatments in certified cancer centres across large populations and different cancer entities in comparison to hospitals that do not hold a certificate. WiZen is a retrospective comparative cohort study that analyzes incident cases of eight types of cancer diagnosed within 2009-2017 based on nationwide health insurance data provided by WIdO (the AOK research institute) and data from regional clinical cancer registries (CCR) for the period 2006-2017. These eight types of cancer are colorectal cancer, pancreatic cancer, breast cancer, gynecologic tumors, lung cancer, prostate cancer, head and neck tumors and neuro-oncological tumors.


Recruitment information / eligibility

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

Study Design


Intervention

Other:
Oncological certification
Oncological certification encompasses a variety of criteria such as treatment according to the clinical guidelines, staffing, technical infrastructure, minimum caseloads, and multidisciplinary care.

Locations

Country Name City State
Germany Technische Universität Dresden Dresden Sachsen

Sponsors (4)

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)

Country where clinical trial is conducted

Germany, 

Outcome

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
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