Rapid Learning for Lung Cancer

Rapid Learning in Practice: A Lung Cancer Survival Decision Support System in Routine Patient Care Data

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01949259

Enrollment

10000

Registered

2013-09-24

Start date

2013-09-30

Completion date

2014-08-31

Last updated

2016-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Retrospective, Lung cancer

Brief summary

A retrospective, data mining project that re-uses routine patient care data for decision support systems.

Detailed description

By installing tools that extract clinical data from electronic health records and image data from the Picture Archiving and Communication System, decision support systems are built and validated that can predict survival and treatment toxicities of lung cancer patients treated with radiotherapy.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

\- Patients notes as suffering from lung cancer in at least one clinical data source.

Design outcomes

Primary

Measure	Time frame	Description
Survival	From radiotherapy until death	Retrospective data will be collected from each included patient from start of radiotherapy until end of study or death (an expected average of 10 years).

Secondary

Measure	Time frame	Description
Local control	From start of treatment until death,	Data will be collected from inclusion in the study until end of study of death (an expected average time frame of 10 years) concerning the local control of this tumour.
Distant metastases	From treatment until end of study	Data concerning the possible occurence of distant metastases will be collected from each patient from inclusion until end of study or date of death (an expected average time frame of 10 years).
Dyspnea	From inclusion until end of study	From each included patient, dyspnea scores will be collected from start of treatment until end of study or date of death (an expected average time frame of 10 years).
Dysphagia	From treatment until end of study	Dysphagia scores will be collected from each participating patient from treatment until end of study or date of death (an average time frame of 10 years)

Countries

Netherlands

Outcome results