NCT07532668

Brief Summary

The goal of this observational study is to describe palliative pathways in adult patients who died from their sarcoma. The main question it aims to answer is: How patients who died from sarcoma are followed by palliative team.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
207

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

March 25, 2026

Completed
22 days until next milestone

First Posted

Study publicly available on registry

April 16, 2026

Completed
Last Updated

April 16, 2026

Status Verified

April 1, 2026

Enrollment Period

1 year

First QC Date

March 25, 2026

Last Update Submit

April 9, 2026

Conditions

Keywords

sarcomapalliative careaggressivness of carecancerend of life

Outcome Measures

Primary Outcomes (1)

  • Palliative pathways of patients who died from sarcoma

    Palliative pathways will be described using the proportion of patients with each of the following component : * hospitalisation in a palliative care unit, * consultation with palliative care doctor, * mobile palliative care team advice We collect data on the first and last time of each kind of palliative follow up, we collect the number of day between the meeting and death For exemple: palliative care unit: first meeting 200 days before death and last meeting 80 days before death

    From date of inclusion until the date of death from any cause, assessed up to 42 months

Secondary Outcomes (7)

  • Treatment with chemotherapy in the last 14 days of life

    From date of inclusion until the date of death from any cause, assessed up to 42 months

  • More than 1 visit in an emergency unit in the last 30 days of life

    From date of inclusion until the date of death from any cause, assessed up to 42 months

  • Hospitalization in a resuscitation unit in the last 30 days of life

    From date of inclusion until the date of death from any cause, assessed up to 42 months

  • More than 1 hospitalization in the last 30 days of life

    From date of inclusion until the date of death from any cause, assessed up to 42 months

  • Less than 3 days in palliative care unit

    From date of inclusion until the date of death from any cause, assessed up to 42 months

  • +2 more secondary outcomes

Study Arms (2)

adult patients who died from sarcoma with >1 agressivness near the end of life criteria

adult patients who died from sarcoma with 0-1 agressivness near the end of life criteria

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients with sarcoma follow up in Centre Léon Bérard, or Institut Gustave Roussy, or Institut Curie who died in 2024

You may qualify if:

  • Oncology follow up in Centre Léon Bérard, or Institut Gustave Roussy, or Institut Curie
  • sarcoma histology confirmed
  • \>18 years at diagnosis
  • death between 01/01/2024 ans 31/12/2024
  • death related to sarcoma

You may not qualify if:

  • \>1 year between last follow up in Centre Léon Bérard, or Institut Gustave Roussy, or Institut Curie and death
  • patient opposed to the collect of data

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Leon Berard

Lyon, France

Location

MeSH Terms

Conditions

SarcomaNeoplasmsDeath

Condition Hierarchy (Ancestors)

Neoplasms, Connective and Soft TissueNeoplasms by Histologic TypePathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 25, 2026

First Posted

April 16, 2026

Study Start

January 1, 2024

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

April 16, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Individual Participant Data must not be shared according to the local regulation

Locations