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Bone Marrow Transplant clinical trials

View clinical trials related to Bone Marrow Transplant.

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NCT ID: NCT03654599 Completed - Depression Clinical Trials

Effects of Digital Stories Intervention on Psychosocial Well-being

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Patients and caregivers undergoing hematopoietic stem cell transplantation often continue to experience anxiety, depression, isolation, and other psychosocial distress. A narrative-based digital stories intervention has shown promise in a pilot study with breast cancer patients in helping to alleviate emotional distress. This study is designed to test digital stories to be viewed and discussed by other HCT patients/caregivers as a psychosocial intervention in a randomized controlled trial and to test the effects of digital stories on how 110 patient and caregiver dyads (N=220) undergoing one of the most rigorous and aggressive treatments cope with treatment-related distress through supportive open dyadic communication and emotional expression.

NCT ID: NCT03530969 Completed - Lymphoma Clinical Trials

Geriatric Communication Skills Training Program for Oncology Clinicians

Start date: May 7, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to learn more about the effects of a training program designed to help doctors communicate better with older patients and their caregivers.

NCT ID: NCT03245788 Completed - Breast Cancer Clinical Trials

Effectiveness of Lay Navigators in Meeting Cancer Patients' Non-Clinical Needs: A Pilot Study

Start date: February 15, 2017
Phase: N/A
Study type: Interventional

The Stanford Cancer Center is undertaking a Transformation Initiative in order to improve the quality of care and care coordination across the continuum of care. The newest innovation is to introduce lay navigators to specified high-need patients. The larger goal of the project is to assess whether lay navigators can address non-clinical patient needs in a timely fashion and appropriately connect them with their clinical team when warranted. It is expected that proactive interaction with patients will decrease patient anxiety/stress related to their cancer and facilitate higher patient engagement and improved management of physical, social,and emotional health. For the pilot project, the smaller goal is to understand: how lay navigator time is used; the types and frequency of issues brought up by patients; resources that patients are given or referred to; type and frequency of mode of contact with patients; and patients' acceptance of navigators based on refusal. An electronic intake form will be used to collect this information so that data can be analyzed regularly to inform changes to the navigator program as needed.

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: NCT03028961 Completed - Clinical trials for Bone Marrow Transplant

Stanford Letter or Traditional Advance Directive in Advance Care Planning in Patients Undergoing Bone Marrow Transplant

BMTSLPRCT
Start date: March 3, 2017
Phase: N/A
Study type: Interventional

The purpose of the proposed research study is to evaluate whether bone marrow transplant patients prefer the Stanford letter advance care planning tool to the standard Advance directive. Completion of advance care planning prior to BMT is very important, but not often done. The investigators believe that the Stanford Letter will be preferred by patients and will allow them to feel more comfortable and share more of their wishes with family members and the medical team.

NCT ID: NCT02665065 Active, not recruiting - Clinical trials for Acute Myeloid Leukemia

Study of Iomab-B vs. Conventional Care in Older Subjects With Active, Relapsed or Refractory Acute Myeloid Leukemia

SIERRA
Start date: June 2016
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to demonstrate the efficacy of Iomab-B, in conjunction with a Reduced Intensity Conditioning (RIC) regimen and protocol-specified allogeneic hematopoietic stem cell transplant (HCT), versus Conventional Care in patients with Active, Relapsed or Refractory Acute Myeloid Leukemia (AML).

NCT ID: NCT02575079 Completed - Clinical trials for Bone Marrow Transplant

Parafilm to Prevent CLABSI in Pediatric Patients Undergoing HCT

Start date: March 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to see if applying parafilm as an external barrier on the central line in children having a bone marrow transplant helps to prevent central line associated bloodstream infection(s) and also to assess the ease of use of parafilm.

NCT ID: NCT02451462 Withdrawn - Clinical trials for Hematopoietic Stem Cell Transplant

Pilot Trial of Zoledronic Acid to Prevent Bone Loss in Hematopoietic Cell Transplant Recipients

Start date: September 2015
Phase: N/A
Study type: Interventional

Patients who undergo bone marrow transplant for different types of cancer are exposed to many treatments such as steroids and whole body radiation. These treatments make the transplant possible but also make their bones weaker and more prone to fractures which can be a source of significant disability and decreased quality of life for cancer survivors. Our trial will investigate whether giving one dose of Zoledronic acid (a commonly used drug given to preserve bone mass in osteoporosis) before bone marrow transplant can protect from the bone loss caused by the transplant procedures. The investigators are also interested in studying the complex interactions of bone, muscle and fat which are greatly affected after bone marrow transplant.

NCT ID: NCT02057289 Terminated - Cancer Clinical Trials

A Pharmacokinetic Study of Pediatric Micafungin Prophylaxis

Micafungin
Start date: January 2014
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to examine the pharmacokinetics (the process by which a drug is absorbed, distributed, metabolized, and eliminated by the body) of micafungin when it is given at 5mg/kg dose to immunocompromised children as anti-fungal prophylaxis. These children are at high risk for developing invasive fungal disease due to their compromised immunity and associated variable degree and duration of neutropenia. Currently, children who receive micafungin are given daily or alternate day dosing. The investigators will give a ONE TIME dose of micafungin and draw PK levels up to 96 hours post-infusion. The investigators goal is to obtain comparable micafungin drug concentrations at the end of 96 hours (4 days) as compared to lower dose at every 24 hour dosing. The investigators dosing proposal is likely to be effective prophylaxis for immunocompromised patients and would broaden its applicability to larger populations.

NCT ID: NCT01735565 Completed - Clinical trials for Bone Marrow Transplant

Neutrophil Extracellular Trap Formation in Patients Undergoing Bone Marrow Transplant

Start date: June 2012
Phase: N/A
Study type: Observational

This is a prospective observational study to determine the point after bone marrow transplant in adults and children at which the neutrophils derived from the transplanted stem cells are competent to form functional neutrophil extracellular traps (NETs). Furthermore, given the importance of platelet function for NET formation, we also plan to examine platelet activation and function as well as the platelet transcriptome using the same clinical samples.