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NCT ID: NCT02530879 Withdrawn - Clinical trials for Laryngopharyngeal Reflux

Comparison of Voice Therapy and Antireflex Therapy in LPR

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

This study will be a prospective, randomized, unblinded but controlled trial. Patients presenting to the Otolaryngology clinic who are diagnosed with laryngopharyngeal reflux disorder related dysphonia and meet inclusion criteria will be eligible to enroll in the study. Subjects will be randomized to one of three treatment arms, voice therapy, anti-reflux therapy, or a combination of voice therapy and anti-reflux therapy. Reflux symptom index (RSI) scores, reflux finding scores (RFS), voice handicap index-10 (VHI-10) scores, and consensus auditory perceptual evaluation-voice (CAPE-V) scores will be compared prior to initiation of therapy as well as at 1, 2, and 3 months following initiation of treatment.

NCT ID: NCT02530606 Withdrawn - Ovarian Carcinoma Clinical Trials

Photoacoustic Imaging in Detecting Ovarian or Fallopian Tube Cancer

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

This pilot clinical trial studies how well photoacoustic imaging works in detecting ovarian or fallopian tube cancer. Photoacoustic imaging is an imaging method that uses lasers to light up tissue, and then converts the light information into ultrasound images. Photoacoustic imaging can provide images of the structure of tissues, as well as their function and the levels of molecules, such as the flow of blood in blood vessels and the level of oxygen in the blood. Photoacoustic imaging may help doctors determine whether a mass is benign (non-cancerous) or cancerous based on the molecular differences between cancer and normal tissue. It may be more accurate and less expensive than other imaging methods, and does not expose patients to radiation.

NCT ID: NCT02530086 Withdrawn - Clinical trials for Small Bowel Obstruction

Prospective Study of Non-operative Management of SBO Without Nasogastric Tube Placement

NoNGT
Start date: August 2015
Phase: N/A
Study type: Interventional

A prospective randomized trial comparing non-operative management of small bowel obstruction due to adhesions with or without a naso-gastric tube (NGT).

NCT ID: NCT02528877 Withdrawn - Clinical trials for Secondary Acute Myeloid Leukemia

Ruxolitinib Phosphate, Tacrolimus and Sirolimus in Preventing Acute Graft-versus-Host Disease During Reduced Intensity Donor Hematopoietic Cell Transplant in Patients With Myelofibrosis

Start date: November 2015
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of ruxolitinib phosphate when given together with tacrolimus and sirolimus in preventing acute graft-versus-host disease during reduced intensity donor hematopoietic cell transplant in patients with myelofibrosis. Sometimes transplanted cells from a donor can attack the normal tissue of the transplant patient called graft-versus-host disease. Ruxolitinib phosphate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. It may also reduce graft-versus-host disease by reducing inflammation and immune modulation. Giving ruxolitinib phosphate together with tacrolimus and sirolimus after transplant may prevent graft-versus-host disease.

NCT ID: NCT02528617 Withdrawn - Clinical trials for Gaucher Disease Type 1

The Effect of Velaglucerase Alfa (Vpriv) on Skeletal Development in Pediatric Gaucher Disease

Start date: July 2015
Phase: Phase 4
Study type: Interventional

The purpose of this trial is to study the effect of Velaglucerase Alfa on skeletal bone development of children with Type 1 or Type 3 Gaucher Disease. In addition, the natural history and neurological status of children with Type 3 Gaucher Disease will be studied.

NCT ID: NCT02527876 Withdrawn - Clinical trials for Exercise, Delayed Control

Exercise, Activity and Smoking in Young Adults

EASY-A
Start date: August 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate how physical activity levels change in young adults when they start a specific exercise program.

NCT ID: NCT02526329 Withdrawn - Clinical trials for Graft Versus Host Disease

Donor Regulatory T Cells in Treating Patients With Visceral Acute Graft-versus-Host Disease After Stem Cell Transplant

Start date: August 6, 2015
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of donor regulatory T cells in treating patients with graft-versus-host disease affecting the liver or gastrointestinal organs (visceral) within 100 days (acute) after undergoing a stem cell transplant. Graft-versus-host disease occurs when donor immune cells infused in a stem cell transplant attack the gut, skin, liver, or other organ systems of the patient. Regulatory T cells are a type of immune cell that may be able to reduce the attack of the donor's immune cells on the patient's normal cells and help treat graft-vs-host disease.

NCT ID: NCT02525913 Withdrawn - Breast Cancer Clinical Trials

Feasibility Study of Cavity Radiofrequency Ablation in ex Vivo Mastectomy Breast Tissue

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

The purpose of this study is to build a device that will consistently ablate (destroy or remove) cavitary breast tissue after a formal breast cancer resection in order to mimic the tissue that is now irradiated after breast cancer lumpectomy. The device would be easier to handle, perform the ablation in less time and by so ablating this margin would avoid the need in many for reoperation to obtain negative margins and based on preliminary data avoid the need for radiation. This would be especially important in poor and rural patients and would lead to decreased costs of treatment in patients with favorable breast cancer.

NCT ID: NCT02525835 Withdrawn - Clinical trials for Systemic Lupus Erythematosus

Tissue Sodium in Autoimmune Disease

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

This pilot study will test the hypothesis that a low sodium diet will decrease sodium (23Na) magnetic resonance imaging-determined skin sodium concentrations in patients with systemic lupus erythematosus (SLE) and improve blood pressure and inflammation

NCT ID: NCT02524639 Withdrawn - Hyperinsulinism Clinical Trials

Sirolimus for the Treatment of Hyperinsulinism

Start date: August 12, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this pilot study is to generate data to assess feasibility of study design/procedures and for formal sample size estimation for a larger multicenter study of the efficacy and safety of sirolimus in infants with medically-unresponsive congenital hyperinsulinism (HI) due to inactivating mutations of adenosine triphosphate-sensitive potassium (KATP) channels.