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NCT ID: NCT02824575 Terminated - Breast Cancer Clinical Trials

Rebastinib Plus Antitubulin Therapy With Paclitaxel or Eribulin in Metastatic Breast Cancer

Start date: July 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of rebastinib when combined with antitubulin therapy with paclitaxel or eribulin in patients with advanced breast cancer.

NCT ID: NCT02824445 Terminated - Clinical trials for Post-Traumatic Stress Disorders

To Evaluate the Efficacy of EEG-guided Magnetic Resonant Therapy in War Veterans With Posttraumatic Stress Disorder

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

After 13 years of war, PTSD has become pervasive in service members. Traditionally it is evaluated by PTSD Checklist Military Version (PCL-M) and treated with cognitive processing therapy, prolonged exposure therapy and medication management with limited success. Repetitive Transcranial Magnetic Stimulation (TMS) has shown efficacy for improving individual cognitive function in the past decades, both in healthy population and in patients with depression. TMS has been approved by the FDA in treatment of major depressive disorder and migraine headaches. Magnetic EEG guided Resonant Treatment (MeRT) is a form of individualized TMS based on member's EEG/ECG input. Investigators propose to use MeRT to treat veterans with war-related PTSD, a syndrome that includes depressive and anxious symptoms; it is likely that MeRT (namely TMS) will be beneficial and comparable to or better than the current FDA approved methods for treating PTSD.

NCT ID: NCT02823470 Terminated - Cystic Fibrosis Clinical Trials

A Pilot Study to Evaluate the Use of Smart Adherence Technology to Measure Lumacaftor/Ivacaftor Adherence in CF Subjects Homozygous for the F508del CFTR Mutation

Start date: June 2016
Phase: Phase 4
Study type: Interventional

The study will evaluate the impact of smart adherence technology for monitoring on lumacaftor/ivacaftor (LUM/IVA) adherence rates among subjects 16 years of age and older with Cystic Fibrosis (CF) who are homozygous for the F508del Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) mutation.

NCT ID: NCT02823327 Terminated - Clinical trials for AIDS-Related Primary Effusion Lymphoma

Clinical and Genomic Factors for Prognosis of AIDS Primary Effusion Lymphoma

Start date: October 11, 2016
Phase:
Study type: Observational

This research trial studies clinical factors and gene expression analysis for prognosis in tissue samples from patients with acquired immune deficiency syndrome (AIDS)-related primary effusion lymphoma. Gathering health information over time and studying samples of tissue from patients in the laboratory may help doctors learn about the prognosis of patients with AIDS-related primary effusion lymphoma.

NCT ID: NCT02823262 Terminated - Breast Cancer Clinical Trials

A Breast Cancer Treatment Decision Aid for Women Aged 70 and Older

Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of this research study is to evaluate a decision aid to help women aged 70 and older decide on treatment for their breast cancer.

NCT ID: NCT02822755 Terminated - Adherence Clinical Trials

Home Exercise Adherence in Physical Therapy

Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of an individualized video recording in improving adherence in home exercise programs for orthopaedic physical therapy patients. Specific aims: 1. Evaluate whether individualized video recordings improve adherence with home exercise programs (HEP) as compared with conventional printed instructions measured by a self-report exercise log. (1-tail analysis)

NCT ID: NCT02820766 Terminated - Osteoarthritis Clinical Trials

Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting

Start date: September 2016
Phase: N/A
Study type: Observational

The primary objective of the study is to determine how the short-term outcome of subjects implanted with the JOURNEY™ II BCS Total Knee System compares to subjects implanted with other PS total knee systems, and to determine if there is a difference in health care resources consumed that may result in economic savings to patients, the facility and/or the payer. To address the study objectives, patient self-assessment questionnaires, and other objective measures of post-operative function and health care resource utilization will be used for data collection.

NCT ID: NCT02820740 Terminated - Epilepsy Clinical Trials

Feasibility Study on LITT for Medical Refractory Epilepsy

Start date: April 21, 2017
Phase: N/A
Study type: Interventional

Multicenter, open-label, prospective designed study to characterize the performance of brain laser interstitial thermal therapy (LITT) ablation using the Monteris NeuroBlate System for the treatment of drug-refractory medial temporal lobe epilepsy in subjects who are candidates for LITT surgery.

NCT ID: NCT02819999 Terminated - Clinical trials for Small Cell Lung Cancer

A Study of Rovalpituzumab Tesirine (SC16LD6.5) in the Frontline Treatment of Patients With Extensive Stage Small Cell Lung Cancer

Start date: October 2016
Phase: Phase 1
Study type: Interventional

The purpose of the study is to test the effect of rovalpituzumab tesirine in the frontline treatment of small cell lung cancer (SCLC).

NCT ID: NCT02819804 Terminated - Clinical trials for Recurrent Adult Acute Lymphoblastic Leukemia

Nivolumab and Dasatinib in Treating Patients With Relapsed or Refractory Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia

Start date: August 17, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to determine the acceptable upper limit dose of nivolumab in combination with dasatinib that may be given to patients with relapsed/refractory philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ ALL). Nivolumab is currently Food and Drug Administration (FDA) approved for other cancers, but has not yet been investigated in Ph+ ALL. Dasatinib is currently FDA approved for the treatment of Ph+ ALL, but has not yet been investigated in combination with nivolumab for this disease. There is evidence that dasatinib not only blocks the Philadelphia chromosome or breakpoint cluster region-Abelson murine leukemia viral oncogene homolog 1 (BCR-ABL) mutation, but also increases the activity of cells in your immune system. Nivolumab increases T cells in your immune system, which allows your immune system to attack the cancer. We think the combination of these drugs will be more effective against your leukemia than either drug used alone.