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Oncologic Disorders clinical trials

View clinical trials related to Oncologic Disorders.

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NCT ID: NCT03426553 Completed - Clinical trials for Hematologic Diseases

Clinical Use of Pathogen Reduced Red Blood Cell Suspension

Start date: January 15, 2018
Phase: Phase 3
Study type: Interventional

The aim of the study is to evaluate the effectiveness and safety of the application of pathogen inactivated RBC suspension in children with oncological and hematological diseases.

NCT ID: NCT03416465 Completed - Oncologic Disorders Clinical Trials

Place of General Medical During Oncology Care Management

MGPEC_Onco
Start date: May 16, 2018
Phase:
Study type: Observational

The Purpose of MGPEC_ONCO is to see if patient consult their general practitioner during the management of their cancer, especially before hospitalization. The study concerns not planned hospitalizations in medicine service. Before leaving hospital, the patient completes the survey, other data are taken in patient record

NCT ID: NCT03272646 Completed - Clinical trials for Nutritional and Metabolic Diseases

Prognostic Performance of the Naples Prognostic Score

NPS
Start date: January 1, 2000
Phase: N/A
Study type: Observational [Patient Registry]

To investigate the prognostic performance of the Naples Prognostic Score in gastric cancer patients undergoing surgery

NCT ID: NCT03168048 Not yet recruiting - Breast Cancer Clinical Trials

Oncologic Therapy Support Via Means of a Dedicated Mobile App

OPTIMISE-1
Start date: July 2017
Phase: N/A
Study type: Interventional

The present single-center prospective exploratory study, conducted at Heidelberg University Hospital, assesses the feasibility of introducing a concept for additional patient care based on a mobile application for patients undergoing radiotherapy. Patients presenting themselves for the irradiation of thoracic or pelvic tumors will be surveyed regarding general performance, treatment-related Quality of Life (QoL) and symptoms and their need to personally consult a physician on a treatment-daily basis by means of a mobile application. The primary endpoint of feasibility will be reached when 80% of the patients have successfully answered 80% of their respective questions scheduled for each treatment day. Furthermore, treatment-related patient satisfaction and diagnosis-related QoL is assessed by PSQ-18 and EORTC questionnaires at the end of radiotherapy and at the first follow-up.

NCT ID: NCT03041571 Withdrawn - Cancer Clinical Trials

Impact of Early Implementation of Narrative Medicine Techniques on Patient Centered Attitudes of Medical Students

Start date: March 1, 2017
Phase:
Study type: Observational

A qualitative study assessing the impact of early narrative medicine practice on Medical Honors Program (MHP) students' attitudes regarding patient-centered interactions, through interviewing patients with chronic or life-limiting illnesses to obtain their illness stories. MHP students will develop a patient narrative for the patients interviewed. These narratives will be edited by the patient, and, with the permission of the patients, may be published as a collection of stories.

NCT ID: NCT03030248 Completed - Clinical trials for Hematologic Diseases

Vancomycin for C Difficile NAAT+/EIA- Hematology Oncology Patients

Start date: June 1, 2018
Phase: Phase 2
Study type: Interventional

This study will randomized hematology oncology patients with active diarrhea and a NAAT positive/toxin EIA negative to either 14 days of oral vancomycin capsules or placebo. The study is designed to include 30 patients (15 per arm). Outcomes will include C. difficile load using qPCR, VRE loads, structural and functional microbiome changes and frequency of bowel movements. All endpoints will be measured at several time points including days 0, 14, 21 and 90.

NCT ID: NCT02484053 Completed - Oncologic Disorders Clinical Trials

Rapid Infusion Rituximab, Hematologic, Oncologic, and Rheumatologic Disorders

Start date: June 2015
Phase: Early Phase 1
Study type: Interventional

Rituximab is frequently used in adult and pediatric cancers, blood disorders, lymphoma (a cancerous growth made up of lymphoid tissue), graft-versus-host-disease (complication that can occur after a stem cell or bone marrow transplant), diseases of the immune system (the cells and substances that protect the body from infection) and rheumatologic conditions. Rituximab works by decreasing or temporarily eliminating a specific type of white blood cell, the B-lymphocyte. Overall, rituximab is generally well tolerated. The likelihood of an infusion-related reaction, or symptoms such as fever, chills, hives, low blood pressure or swelling, is very low, but highest during a patient's first infusion of rituximab and decreases with each additional dose. Adults commonly receive rituximab at a faster rate if they have done well with the first infusion, this study will help determine if the same approach is well tolerated in children. In this study, the investigators are testing a new method of administering rituximab which may reduce the time it takes to receive the medication. The initial ordered amount of rituximab will not change from the current standard of care (meaning what is usually done by doctors, and would likely be done if you were not on this study). The period of time over which rituximab is given is what is being studied.

NCT ID: NCT02285296 Terminated - Tumor Clinical Trials

The Needs and Burden of Family Caregivers of Older Adults With Cancer

Start date: December 11, 2014
Phase: N/A
Study type: Interventional

Elderly cancer patients need more help from their relatives and for longer than young adults. Our hypothesis of research is that the needs and resources to help the couple " elderly patient/caregiver ", are at least in part socially determined and that the implementation of a personalized support plan to help the caregiver (PSP) taking into account needs, resources and expectations of the primary caregiver in addition to those of elderly patients with cancer may partly correct inequalities. The PSP should allow a better management of cancer, a lesser burden for the caregiver and a better quality of life for both the caregiver and the patient.

NCT ID: NCT01210716 Completed - Autoimmune Diseases Clinical Trials

Evaluation of Therapeutic Plasma Exchange (TPE) Procedure Using the AMICUS Device

Start date: September 2010
Phase: Phase 3
Study type: Interventional

This study will evaluate the use of the AMICUS device in patients where Therapeutic Plasma Exchange (TPE) is prescribed by their physicians.