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SarcomaSARCOPALLNCT07532668

Multicentre Retrospective Cohort Study of Palliative Care Pathways in Patients Who Died From Sarcoma

An observational study of Sarcoma, run by Centre Leon Berard at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Sarcoma
How many people
207 participants
Where
1 siteFrance
Study dates
1 Jan 2024to 31 Dec 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

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

Who may be able to join

  • 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

Who cannot join

  • >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

Trial locations and contacts

1 site in 1 country.

France1 site
  • Centre Leon Berard

    Lyon

Other trials in France

About this study

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.

Conditions
Sarcoma
Keywords
sarcoma, palliative care, aggressivness of care, cancer, end of life
Medical subject headings
Sarcoma, Neoplasms, Death

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07532668
Study groupRoleWhat they receive
adult patients who died from sarcoma with >1 agressivness near the end of life criteriaNot described
adult patients who died from sarcoma with 0-1 agressivness near the end of life criteriaNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

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

Secondary outcomes (7)
  1. Treatment with chemotherapy in the last 14 days of life

    Percentage and number of patients having a treatment with chemotherapy in the last 14 days of life

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

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

    Percentage and number of patients having more than 1 visit in an emergency unit in the last 30 days of life

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

  3. Hospitalization in a resuscitation unit in the last 30 days of life

    Percentage and number of patients having a hospitalization in a resuscitation unit in the last 30 days of life

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

  4. More than 1 hospitalization in the last 30 days of life

    Percentage and number of patients having more than 1 hospitalization in the last 30 days of life

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

  5. Less than 3 days in palliative care unit

    Percentage and number of patients having a hospitalization in a palliative care unit less than three days before death

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

  6. New chemotherapy regimen starting in the last 30 days of life

    Percentage and number of patients having a new chemotherapy regimen starting in the last 30 days of life

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

  7. Place of death

    Hospital and type of unit or home will be described

    Measured: At the date of death from any cause, assessed up to 42 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Apr 2026
  2. Study start1 Jan 2024
  3. Primary completion31 Dec 2024
  4. Study completion31 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
207 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07532668
Sponsor's protocol ID
ET25-182 (SARCOPALL)
Acronym
SARCOPALL
Status last verified
Apr 2026
First submitted
25 Mar 2026
Last updated
16 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual Participant Data must not be shared according to the local regulation

Questions about this trial

What is this clinical trial studying?

An observational study of Sarcoma, run by Centre Leon Berard at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Palliative pathways of patients who died from sarcoma (time frame: From date of inclusion until the date of death from any cause, assessed up to 42 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2026.

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