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NCT ID: NCT01969942 Withdrawn - Ewing Sarcoma Clinical Trials

A Phase I Study to Examine the Toxicity of Allogeneic Stem Cell Transplantation for Relapsed or Therapy Refractory Ewing Sarcoma

ASCT
Start date: April 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine the toxicity of using allogeneic stem cell transplantation for treatment of subjects with relapsed or refractory Ewing Sarcoma (ES). Donors will consist of either Human Leukocyte Antigen identical (HLA)or 9/10 (A, B, C, DR, DQ [A, B, C, are Class I markers for HLA and DR and DQ are Class II markers for Matching for Transplant for Donors to match with recipient]) matched related or unrelated donors. Specifically, we will examine: - The toxicity of allogeneic stem cell transplant (SCT) in this patient population, as related to incidence of grade 3-4 acute Graft Verse Host Disease (GVHD). - The incidence of transplant related mortality at 100 days.

NCT ID: NCT01969682 Withdrawn - Clinical trials for Non-Hodgkin's Lymphoma

A Study to Assess the Effect of Rifampin on the Metabolism of ABT-199

Start date: April 2014
Phase: Phase 1
Study type: Interventional

This is an open-label multicenter, study to assess the pharmacokinetic interaction of rifampin with ABT-199 in up to 12 subjects with relapsed or refractory non-Hodgkin's lymphoma.

NCT ID: NCT01968629 Withdrawn - Clinical trials for Hepatocellular Carcinoma

24hr Imaging Of HCC After EOVIST

Start date: December 2013
Phase: Phase 0
Study type: Interventional

In this research study, the investigators are looking to see if MR imaging with Eovist performed 24 hours after the injection of Eovist helps improve the identification and characterization of focal liver tumors.

NCT ID: NCT01967927 Withdrawn - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Understanding GRID Radiation Therapy Effects on Human Tumor Oxygenation and Interstitial Pressure to Increase Translation of Solid Tumor Therapy

Start date: December 2013
Phase: Early Phase 1
Study type: Interventional

To estimate the mean and standard deviation (SD) of the post-treatment decreases in the interstitial fluid pressure and hypoxia-specific PET-scan signal from GRID-treated tumors in patients with locally advanced squamous-cell carcinoma of the head and neck. The possible effects of GRID radiotherapy on tumor oxygenation levels and interstitial fluid pressure within the tumors will be measured by assessing the trend and statistical significance of the difference in values for each condition obtained prior to and just after GRID exposure in each subject enrolled in the study. We expect that there may be a trend for increases in tumor oxygenation and decreases in interstitial fluid pressure which would indicate that more accurately timed additional chemotherapy and radiation therapy would improve overall patient outcomes.

NCT ID: NCT01967017 Withdrawn - Pain Control Clinical Trials

Study of Local Anesthesia as a Method to Decrease IUD Insertion Related Pain

Start date: June 2014
Phase: Phase 4
Study type: Interventional

Despite the high efficacy of intrauterine devices (IUDs), some women choose not to receive IUDs secondary to the pain associated with insertion. Nulliparous women may be especially susceptible to procedure-related pain from IUD insertion. This study will investigate the difference in perceived pain from IUD insertion, comparing local anesthesia to a placebo, among women who have not had a vaginal delivery before. The investigators anticipate that among women who have not had a previous vaginal delivery, the pain associated with IUD insertion will be significantly decreased after administration of local anesthesia.

NCT ID: NCT01966341 Withdrawn - Clinical trials for Irritable Bowel Syndrome (IBS)

Collaborative Cognitive Behavioral Therapy / Hypnotherapy for Treatment of Pediatric Functional Gastrointestinal Disease

CAPP
Start date: April 2014
Phase: N/A
Study type: Interventional

This program has been created to help patients with irritable bowel syndrome manage their symptoms and increase their functioning by using cognitive therapy skills and hypnosis.

NCT ID: NCT01965041 Withdrawn - Clinical trials for Pattern Dystrophy of Macula

Intravitreal Aflibercept Injections In The Treatment Of Pattern Dystrophy

AVA
Start date: October 2013
Phase: N/A
Study type: Interventional

Adult-onset vitelliform detachments associated with pattern dystrophy is a genetic disorder that carries visual implications that most commonly affect the macula (area in the eye near the retina that is essential for sharp central vision). Adult onset vitelliform detachments have an accumulation of material on the outer retina. Over time, the abnormal accumulation of this material can damage cells that are critical for clear central vision. As a result, people with this disorder often lose their central vision, and their eyesight may become blurry or distorted.

NCT ID: NCT01964235 Withdrawn - Clinical trials for Advanced Hepatocellular Carcinoma

Study of Efficacy and Safety INC280 in Patients With Advanced Hepatocellular Carcinoma

Start date: December 2016
Phase: Phase 2
Study type: Interventional

This study is establish whether INC280 is safe and has beneficial effects in patients with advanced hepatocellular carcinoma known to have dysregulation of c-MET pathway and whose disease progressed while on, or after, treatment with sorafenib or who are intolerant to sorafenib. Patients will be randomized in a 2:1 ratio to receive INC280 at 600mg BID plus best supportive care (BSC) or placebo plus BSC, until disease progression or intolerable to study treatment. Patients treated with placebo plus BSC will have the opportunity to receive INC280 treatment upon documented further disease progression (RECIST 1.1) per investigator's discretion after unblinding. Patient will be stratified to geographical region (Asia vs Rest of World ) and tumor burden (present macroscopic vascular invasion and/or extra-hepatic spread vs not present).

NCT ID: NCT01963832 Withdrawn - Clinical trials for Severe Stroke With Affected Arm Motor Function

RCT of a Neuroplasticity Agent and CI Therapy for Severe Arm Paresis After Stroke

Start date: November 2016
Phase: Phase 2
Study type: Interventional

Stroke patients who have little or no voluntary movement in the hand on the more affected side of their body more than one year after stroke have few treatment options. This project proposes to test the efficacy of a form of Constraint-Induced Movement therapy designed for patients with such severe impairment in conjunction with an agent, fluoxetine, which has been shown in some studies to enhance brain neuroplasticity in response to training. Constraint-Induced Movement therapy, which is abbreviated CIMT, is a form of physical rehabilitation based on basic research in neuroscience and behavioral science. If the project is successful, an efficacious, evidence-based therapy will become available to stroke patients for what is now a largely untreated condition

NCT ID: NCT01961934 Withdrawn - Gliomas Clinical Trials

C11-Sodium Acetate PET/CT Imaging Evaluation in Brain Glioma, Post Therapy Necrosis and Pseudo-progression

Start date: May 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This study will investigate how well Carbon Acetate PET/CT imaging helps to correctly identify recurrent tumor versus post treatment effects (radionecrosis) in patients with previously treated high grade brain gliomas.