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NCT04089306 Clinical Trial

Integration of Palliative Care in an Oncology and Hematology Unit

Advanced Cancer Clinical Trial

Official title:
Integration of Palliative Care in an Oncology and Hematology Unit : a Retrospective Monocentric Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04089306
Other study ID # 7424
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 1, 2019
Est. completion date May 2020

Study information
Verified date April 2019
Source University Hospital, Strasbourg, France
Contact Gabriel MALOUF, MD, PhD
Phone 03 88 11 62 22
Email gabriel.malouf@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main goal of this study is to assess retrospectively the integration of Palliative Care in an oncology and hematology unit. The investigators will study the last six month of life on advanced cancer patients and retrieve data from their medical file to obtain criterias of quality of care and integration of palliative care in this population.

Those criterias have been used before in other setting (Earle Criterias, ESMO Recommendations) and The investigators will compare our data to existing publications.

They also hope to see if it is retrospectively possible to assess the probability of death using the Pronopall score. This will help them asses if aggressive end of life care could have been avoided using the Pronopall Score

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date May 2020
Est. primary completion date May 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient aged over 18 years old

- Patient who has been followed in the oncohematology Unit of the University Hospital of Strasbourg for a solid tumor or haematological cancer

- Died within the 1rst of January 2017 and the 31st of December 2018

- The patient has not expressed an opposition to the use of his medical data during his lifetime.

Exclusion Criteria:

- Patient receiving allogeneic stem cell transplant

- Patient expressed during his lifetime an opposition regarding the use of his medical data

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service D'Hematologie Et D'Oncologie Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Retrospective study of palliative care in oncohematology department The period from January 1st, 2017 to December 31, 2018 will be examined
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