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Regional Database for Collecting Clinical-biological and Imaging Data "Secondary Bone Oncology and Bone Localizations of Hematologic Diseases"

Regional Database for Collecting Clinical-biological and Imaging Data "Secondary Bone Oncology and Bone Localizations of Hematologic Diseases"

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05495802
Acronym
OOSLOH
Enrollment
0
Registered
2022-08-10
Start date
2026-12-01
Completion date
2032-12-01
Last updated
2026-05-15

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

Conditions

Bone Metastases

Keywords

bone localisations of haematological diseases, Cancer, bone metastasis, haematological diseases, quality of life, epidemiological data

Brief summary

Improving the effectiveness of cancer treatments makes it possible to lengthen patient survival. It is therefore important to ensure that the quality of life is also maintained by reducing pain and handicap. Some cancers tend to spread to the bone. The bone locations of cancer can weaken the bone and lead to complications such as fractures, pain, or compression of neurological structures. To avoid such complications, weekly multidisciplinary meetings (MM) bring together specialists (oncologists, rheumatologists, cancer surgeons, radiologists, radiotherapists, etc.) to discuss the files of patients with bone lesions from cancer. They offer specific treatments adapted to each patient to treat or reduce the risk of complications. The OOSLOH study aims to collect clinical, biological, and imaging data from patients for whom a discussion took place in bone dedicated MM. Based on these data, epidemiological studies could be carried out to better understand the clinical factors leading cancer to colonize bone. But also to determine the factors making it possible to prevent or better treat bone complications and improve the quality of life of patients. This study does not require any examinations or additional visits to the patient

Interventions

None listed

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient aged 18 or over, * Patient whose file is presented to the OOSLOH MM and who has not objected to the use of his non-nominative clinical, biological and imaging data * Social insured patient

Exclusion criteria

* Patient who died before presentation to OOSLOH MM, * Minor patient, * Patient objecting to the use of their data for research purposes, * Patient unable to express his right to object to his participation in the study.

Design outcomes

Primary

MeasureTime frame
Percentage of alive patientsthrough study completion, an average of 10 years

Secondary

MeasureTime frame
Percentage of patients without bone disease recurrencewithin one year after the multidisciplinary meeting
Time to bone disease recurrencethrough study completion, an average of 10 years
Number of bone recurrence Number of bone recurrenceAt each presentation of the patient file's to the MM,on average every week
Epidemiological datasAt the first presentation of patient's file to the MM, on average every week

Contacts

PRINCIPAL_INVESTIGATORMarie-Hélène VIEILLARD, MD

University Hospital, Lille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 16, 2026