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NCT ID: NCT03576495 Completed - Clinical trials for Patient-reported Satisfaction With Resident Physicians Involved in Their Care

The Provider Awareness and Cultural Dexterity Toolkit for Surgeons Trial

PACTS
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

This study is designed to test the impact of a new curriculum, called Provider Awareness Cultural Dexterity Toolkit for Surgeons (PACTS), on surgical residents' cross-cultural knowledge, attitudes, and skills surrounding the care of patients from diverse cultural backgrounds, as well as clinical and patient-reported health outcomes for patients treated by surgical residents undergoing this training.

NCT ID: NCT03576469 Completed - Clinical trials for CVI - Common Variable Immunodeficiency

A Study to Evaluate the Benefit of RUCONEST® in Subjects Who Experience ADRs Related to IVIG Infusions

Start date: June 13, 2018
Phase: Phase 4
Study type: Interventional

Patients receiving intravenous immunoglobulin (IVIG) therapy for primary immunodeficiency and neurologic conditions may experience adverse drug reactions (ADRs). The mechanism of the ADR is unknown. Currently, the standard practice for these patients is to change from IV to subcutaneous IG (SCIG) but because of the need of immunomodulation or patient preference, SCIG may not be an option. Data has shown that some levels of complement decrease from pre- to post-infusion of IVIG. This study is to determine if replacing this complement protein may ameliorate ADRs.

NCT ID: NCT03576183 Completed - Diarrhea Clinical Trials

Study Confirming A Human Challenge Model and Investigating The Safety Of VLA1701

Start date: June 4, 2018
Phase: Phase 2
Study type: Interventional

This is a single-center, double-blind, placebo-controlled, Phase II vaccination and challenge study designed to confirm a human challenge model with E. coli strain LSN03-016011/A.

NCT ID: NCT03576157 Completed - Breast Feeding Clinical Trials

Kilkari Impact Evaluation

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

British Broadcasting Corporation (BBC) Media Action is presently implementing two large scale mobile health (mHealth) initiatives in India: Kilkari and Mobile Academy. Kilkari is an outbound service that delivers weekly, time-appropriate audio messages about pregnancy, childbirth, and childcare directly to families on their mobile phones, starting from the second trimester of pregnancy until the child is one-year-old. Mobile Academy (MA) is an Interactive Voice Response (IVR) in-service audio training course for Accredited social health activists (ASHAs) in India designed to refresh their knowledge of life-saving preventative health behaviors and improve their interpersonal communications skills. Both programs were initiated in Bihar in 2012, and have been scaled widely in a number of states with support from Ministry of Health and Family Welfare (MOHFW) at the national level, National Health Missions (NHM) at the state level, and an alliance of donors (Gates Foundation, USAID, Barr Foundation, and UK Department for International Development (UKAid)). The Johns Hopkins School of Public Health, Oxford Policy Management, and University of Cape Town are supporting BBC Media Action and the Ministry of Health and Family Welfare (MOHFW) are conducting an external evaluation of both Kilkari and Mobile Academy (MA). The evaluation spans through April 2020.

NCT ID: NCT03576092 Completed - Clinical trials for Pregnancy Complications

Lung Ultrasound Patterns Preeclampsia

Start date: August 15, 2016
Phase:
Study type: Observational

Evaluation of lung ultrasound as a diagnostic tool in pregnant patients.

NCT ID: NCT03576079 Completed - Clinical trials for Temporomandibular Joint Disorders

Effect of Laser Therapy Versus Anterior Re-positioning Splint in the Treatment of Disc Displacement With Reduction

Start date: September 1, 2015
Phase: N/A
Study type: Interventional

comparing the effects of Laser therapy with anterior re-positioning splint and a placebo group on clinical signs and symptoms of temporo-mandibular dis-function and assessing articular disc morphology and configuration with magnetic resonance imaging.

NCT ID: NCT03575949 Completed - Clinical trials for Metastatic Head and Neck Squamous Cell Carcinoma

Standard and Delayed FDG PET/CT After Chemoradiation Therapy in Assessing Patients With Metastatic Head and Neck Squamous Cell Cancer

Start date: June 15, 2018
Phase: N/A
Study type: Interventional

This trial studies how well standard and delayed fludeoxyglucose F-18 (FDG)-positron emission tomography (PET)/computed tomography (CT) given after standard radiation and chemotherapy works in assessing patients with head and neck squamous cell cancer that has spread to other places in the body. Diagnostic procedures, such as PET/CT, use radioactive material, such as fludeoxyglucose F-18, to find and diagnose head and neck tumors and may help to find out how far the disease has spread.

NCT ID: NCT03575767 Completed - Clinical trials for Graft Vs Host Disease

Characteristics and Dynamics of TCR Repertoire in Patients With Hematological Malignancies After Allo-HSCT

Start date: May 8, 2018
Phase:
Study type: Observational [Patient Registry]

Graft-versus-Host Disease (GVHD) and relapse, which is mainly due to lack of Graft-versus-Leukemia (GVL), are the most frequent and severe complications of allogeneic hematopoietic stem cell transplantation (allo-HSCT). T cells expanded from mature T cells in the graft play a dominant role in development of GVHD and GVL early after allo-HSCT. Recent applications of high-throughput sequencing (HTS) to the T cells repertoire open a new avenue for us to look deeply into how these T cells dynamically adjust in the context of the recipient's environment. The main goal of this research study is to set up a mathematical model based on T cell receptor (TCR) sequencing to enable prediction for the key immunologic outcomes early post-transplantation. This study will deepen the understanding of the molecular mechanisms driving the most deadly post-transplantation complications, and serve as convincing evidence upon which to choose a better donor and a more proper transplantation approach. This observational trial will perform HTS for TCR β-chain complementarity determining region 3 (CDR3) repertoires of grafts and peripheral blood samples from recipients post-transplantation and analyze the relationship between dynamics of TCR CDR3 repertoires and clinical outcomes early post-transplantation, especially including GVHD and relapse. The investigators want to know how the antigen environment in recipients drives dynamics of mature T cells from grafts in order to use the new discovered rules to better predict and treat the disease process.

NCT ID: NCT03575598 Completed - Clinical trials for Squamous Cell Carcinoma of the Oral Cavity

Sitravatinib (MGCD516) and Nivolumab in Oral Cavity Cancer Window Opportunity Study

SNOW
Start date: August 30, 2018
Phase: Early Phase 1
Study type: Interventional

This is a window of opportunity study for patients with resectable squamous cell carcinoma of the oral cavity who are considered suitable for curative-intent surgical resection, with pre-operative drugs, Sitravatinib and Nivolumab.

NCT ID: NCT03575325 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Vyxeos(CPX-351) in Adults w R/R Acute Lymphoblastic Leukemia

Start date: October 11, 2018
Phase: Phase 2
Study type: Interventional

This study involves Vyxeos (CPX-351), a formulation of a fixed combination of the two anti-tumor drugs, cytarabine and daunorubicin that will be given as an infusion over 90 minutes. This study will use what is called a "liposome" injection. This is a special fat capsule (called a liposome) that surrounds the cytarabine and daunorubicin and protects the drugs from being eliminated/destroyed by the body.