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ong-term Patient Related OuTcomEs in lung Cancer Treatment (PROTECT): Influence of patient decisions on QOL, functionality and survival.

Recruiting
Conditions
lung cancer
10029107
Registration Number
NL-OMON46656
Lead Sponsor
Medisch Centrum Leeuwarden
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
500
Inclusion Criteria

Newly diagnosed stage III or IV lung cancer, both histopathological proven as clinical diagnosis in patients not able to undergo invasive diagnostics.
Patients must be able to understand and complete protocol requirements, Instructions, and questionnaires provided in Dutch

Exclusion Criteria

First line of cancer treatment for stage III or IV started in another hospital

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Primary endpoint<br /><br>1) QOL as assessed by questionnaires (QLQ-C30, QLQ-LC13) (sum scores and<br /><br>different subdomains). </p><br>
Secondary Outcome Measures
NameTimeMethod
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