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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05495802
Other study ID # 2019_59
Secondary ID 2021-A00829-32
Status Not yet recruiting
Phase
First received
Last updated
Start date December 2022
Est. completion date December 2032

Study information

Verified date August 2022
Source University Hospital, Lille
Contact Marie-Hélène VIELLARD, MD
Phone 0320445962
Email Marie-Helene.VIEILLARD@chu-lille.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 5000
Est. completion date December 2032
Est. primary completion date November 2032
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Lille Lille University Hospital Emergence Fund

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of alive patients through study completion, an average of 10 years
Secondary Percentage of patients without bone disease recurrence within one year after the multidisciplinary meeting
Secondary Time to bone disease recurrence through study completion, an average of 10 years
Secondary Number of bone recurrence Number of bone recurrence At each presentation of the patient file's to the MM,on average every week
Secondary Epidemiological datas At the first presentation of patient's file to the MM, on average every week
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