Multimodality Treatment Including Curative Resection of Advanced NSCLC

NCT ID: NCT04455984

Last Updated: 2020-07-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

190 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-05-01

Study Completion Date

2020-08-01

Brief Summary

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This study retrospectively evaluates clinical parameters and outcome of patients with advanced stage non-small cell lung cancer treated with neoadjuvant therapy followed by curative-intent surgery at the Divison of Thoracic Surgery at the Medical University of Vienna

Detailed Description

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This study will be undertaken as a retrospective cohort study at Devision of Thoracic Surgery, Medical University of Vienna. All patients with non-small-cell lung cancer, who received an induction chemo- or chemoradiotherapy followed by surgery in a curative intention at the Devision of Thoracic Surgery, Medical University, will be included. The aim of this study is to evaluate peri- and postoperative clinical parameters and short- and long-term outcomes in patients.

Conditions

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Advanced Non-small-cell Lung Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Neoadjuvant chemoradiotherapy

Patients with advanced NSCLC treated with neoadjuvant platinum-based chemoradiotherapy followed by curative-intent surgery

Date collection

Intervention Type OTHER

Retrospective data analysis

Neoadjuvant chemotherapy

Patients with advanced NSCLC treated with neoadjuvant platinum-based chemotherapy followed by curative-intent surgery

Date collection

Intervention Type OTHER

Retrospective data analysis

Interventions

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Date collection

Retrospective data analysis

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with advanced NSCLC and multimodality treatment including curative-intent resection

Exclusion Criteria

* Patients with early stage NSCLC
* Patients with advanced NSCLC without multimodality treatment
* Patients without curative resection
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medical University of Vienna

OTHER

Sponsor Role lead

Responsible Party

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Katharina Sinn

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medical University of Vienna

Vienna, , Austria

Site Status RECRUITING

Countries

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Austria

Central Contacts

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Katharina Sinn, MD

Role: CONTACT

004314040056440

Facility Contacts

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Katharina Sinn, MD

Role: primary

Other Identifiers

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193132122

Identifier Type: -

Identifier Source: org_study_id

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