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Malignant Lymphoma clinical trials

View clinical trials related to Malignant Lymphoma.

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NCT ID: NCT04986293 Recruiting - Esophageal Cancer Clinical Trials

CPAP or BiPAP for Motion Mitigation During Radiotherapy

SISTER
Start date: June 1, 2021
Phase: N/A
Study type: Interventional

When using highly conformal radiotherapy techniques, such as proton therapy, a controlled breathing pattern and a minimal breathing amplitude could greatly benefit the treatment of mobile tumors. This reduction in tumor motion may be achieved with the use of a ventilator that is able to regulate and modulate the breathing pattern. CPAP provides a constant level of positive airway pressure. Compared to spontaneous breathing, the use of CPAP increased lung volume and can result in a significant decrease in tumor movement and a significant decrease in both mean lung and mean heart radiation dose. These results were found in patients treated for limited stage disease, it is not clear if this approach is feasible for patients with more advanced stage of disease that undergo radiotherapy with curative intent. With Bilevel Positive Airway Pressure (BiPAP), tidal volume excursions are determined by the pressure difference between the set inspiratory positive airway pressure (IPAP) and the set expiratory positive airway pressure (EPAP). This mode of ventilation increases lung volume comparable to CPAP, but also to control tidal volumes and breathing frequency. However, BiPAP has never been studied in the setting of motion mitigation during radiotherapy and BiPAP might be more difficult to adjust to for patients compared to CPAP. Therefore, the current study is proposed to evaluate whether or not CPAP or BiPAP is of benefit in patients that undergo radiotherapy for larger intra-thoracic tumor volumes.

NCT ID: NCT04698616 Recruiting - Malignant Lymphoma Clinical Trials

Lean Body Mass and Side Effects in Patients With Lymphoma

Start date: February 9, 2020
Phase:
Study type: Observational

The primary purpose is to investigate the relationship between the dose of chemotherapeutic agents per kilogram of lean body mass (LBM) and the development of side effects induced by chemotherapy in patients with lymphoma. Secondarily, the maximum tolerable dose of chemotherapeutics (MTD), patients' quality of life (QOL), nutritional status and physical activity during the course of treatment are estimated.

NCT ID: NCT03062072 Recruiting - Breast Cancer Clinical Trials

Emergence of Chemotherapy Related Hyperglycemia in nOn-diabetic Patients

ECHO
Start date: April 2015
Phase: N/A
Study type: Observational

To assess chemotherapy related hyperglycemia in non-diabetic patients, the investigators will assess the incidence of hyperglycemia and analyze co-medications and risk factors.

NCT ID: NCT02131688 Recruiting - Malignant Lymphoma Clinical Trials

Phase I Study of Mitoxantrone Hydrochloride Liposome Injection

Start date: May 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose,the safety and effectiveness of Mitoxantrone Hydrochloride Liposome Injection.