Clinical Impact of Thoracic Scanographic Characteristics of Hematologic Malignancy Patients
Launched by UNIVERSITY HOSPITAL, TOULOUSE · Jan 12, 2023
Trial Information
Current as of July 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying patients with certain blood cancers who are experiencing symptoms related to a condition called mediastinal mass syndrome (MMS). MMS can happen when a mass in the middle of the chest puts pressure on nearby organs, leading to various symptoms like trouble breathing or issues with blood vessels. The trial aims to gather information about how these patients are diagnosed and treated, especially those who are admitted to the Intensive Care Unit (ICU) either for the first time or during a relapse of their cancer.
To participate in the trial, patients must have a blood cancer and show symptoms of MMS, and they need to be admitted to the ICU for their symptoms. They should have had a chest CT scan within a specific timeframe after receiving a certain amount of steroid treatment. The researchers hope to learn more about the best ways to manage these patients quickly and safely. Participants can expect to undergo tests and procedures to help doctors understand their condition better, and their experiences will contribute valuable information to improve future care for others facing similar challenges.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Hematologic malignancy at diagnosis or relapse
- • Symptomatic mediastinal mass syndrome
- • Admission to the ICU, Continuous Medical Surveillance (CMS) or Intensive Care (IC) for symptomatology related to MMS
- • Chest CT (after maximum 48 hours of corticosteroid therapy (1mg/kg/ Prednisone equivalent), maximum 15 days before and 5 days after admission to ICU)
- • Maximum administration of corticosteroid therapy 48 hours before admission to the ICU (maximum 1mg/kg/ Prednisone equivalent)
- • No prior pleural or pericardial drainage
- • Study period: 01/01/2014 - 31/12/2021 (8 years)
- Exclusion Criteria:
- • No diagnosis of hematologic malignancy
- • Diagnosis of solid benign or malignant tumor
- • No mediastinal mass syndrome
- • No admission to ICU/CMS
- • No chest CT scan meeting inclusion criteria
- • Administration of corticosteroids for more than 48 hours prior to admission to the ICU and/or prior to chest CT
- • Lack of social security affiliation.
About University Hospital, Toulouse
The University Hospital of Toulouse is a leading academic medical center dedicated to advancing healthcare through innovative research and clinical trials. With a strong emphasis on patient-centered care, the hospital integrates cutting-edge scientific inquiry with comprehensive clinical services. Its multidisciplinary team of healthcare professionals collaborates with renowned researchers to facilitate pioneering studies across various medical fields, aiming to enhance treatment options and improve patient outcomes. As a prominent institution in the region, the University Hospital of Toulouse is committed to fostering an environment of excellence in both education and research within the healthcare community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Toulouse, , France
Patients applied
Trial Officials
Muriel Picard, MD
Principal Investigator
University Hospital, Toulouse
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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