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NCT ID: NCT02253394 Terminated - Clinical trials for Pulmonary Arterial Hypertension

The Combination Ambrisentan Plus Spironolactone in Pulmonary Arterial Hypertension Study

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

The purpose of this study is to find out if spironolactone added to ambrisentan for Pulmonary Arterial Hypertension (PAH) will increase exercise capacity. We also want to find out if spironolactone and ambrisentan effect the cardiac output (amount of blood the heart pumps every minute), right ventricle function and quality of life.

NCT ID: NCT02252796 Terminated - Clinical trials for Non-small Cell Lung Cancer

Phase I Hypofractionated Stereotactic Boost (Radiotherapy) for Non-Small Cell Lung Cancer

HySBst
Start date: July 2014
Phase: Phase 1
Study type: Interventional

This study will help researchers test the safety of hypofractionated dose of radiotherapy (HySBst) at different dose levels before or after chemo-radiation for Non Small Cell Lung Cancer.

NCT ID: NCT02252432 Terminated - Laminectomy Clinical Trials

The Effects of Ketamine and Methadone on Postoperative Pain for Laminectomy

Start date: February 2013
Phase: Phase 4
Study type: Interventional

The purpose of this research is to determine the pain-reducing effects of ketamine (Ketalar, an FDA-approved drug for anesthesia) and methadone (Dolophine, a long-acting narcotic) after lumbar laminectomy. The investigators would like to evaluate whether intraoperative use of both drugs may be able to provide better control of pain after lumbar surgery.

NCT ID: NCT02250313 Terminated - Prostate Cancer Clinical Trials

PASCUAL (Prostate Assay Specific Clinical Utility at Launch) Study

PASCUAL
Start date: September 2014
Phase:
Study type: Observational

The main hypothesis of this study is to demonstrate that the use of the ConfirmMDx for Prostate Cancer test in previously biopsied patients improves urologists' patient management by reducing unnecessary repeat biopsies, attendant procedure costs, and potential adverse events in men being considered for a repeat procedure.

NCT ID: NCT02250183 Terminated - Burns Clinical Trials

Medihoney and Santyl for Burn Injuries

MSBI
Start date: March 15, 2014
Phase: N/A
Study type: Interventional

This study is designed to assess the efficacy of MEDIHONEY® Gel with Active leptospermum honey dressing relative to SANTYL® ointment dressing on time to heal, bacterial growth in the wound, patient satisfaction, and treatment costs in patients with partial thickness burns. The study has four hypotheses: 1. It is hypothesized that MEDIHONEY® Gel with Active leptospermum honey will result in significantly faster wound healing (i.e., fewer days) when compared to SANTYL®. 2. It is hypothesized that MEDIHONEY® Gel with Active leptospermum honey sites will yield significantly fewer positive cultures for Pseudomonas aeruginosa and other bacteria when compared to SANTYL® sites. 3. It is hypothesized that patients will provide significantly higher patient care satisfaction ratings regarding their MEDIHONEY® Gel with Active leptospermum honey sites when compared to ratings with regard to their SANTYL® sites. 4. It is hypothesized that treatment costs, across participants, will be significantly lower for MEDIHONEY® Gel with Active leptospermum honey than for SANTYL®.

NCT ID: NCT02249819 Terminated - Stroke Clinical Trials

Evaluating Anodal tDCS Preceding Aphasia Therapy

Start date: September 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if non-invasive brain stimulation (transcranial direct current stimulation) delivered prior to language therapy will improve word-finding in individuals with aphasia who are 6 months or greater post-stroke.

NCT ID: NCT02249559 Terminated - Parkinsons Disease Clinical Trials

Pilot Study Evaluating Safety of Unilateral Gamma Knife Subthalamotomy for Parkinson's Disease

GKSTN
Start date: July 2014
Phase: N/A
Study type: Observational

This is a pilot study to evaluate the safety and efficacy of unilateral gamma knife subthalamotomy for Parkinson's disease in patients deemed poor candidates for deep brain stimulation.

NCT ID: NCT02249377 Terminated - Baker's Cyst Clinical Trials

PRP vs Corticosteroid in Baker's Cyst

Start date: February 2014
Phase: Phase 3
Study type: Interventional

This is a Prospective study with Randomized patients into either Ultrasound-guided Platelets-Rich-Plasma injection and Ultrasound guided Corticosteroid Injection, with 3 months and 6 months follow ups after aspiration at our institution. There will be 25 patients in each group, including any patient with symptomatic baker's cyst.

NCT ID: NCT02248740 Terminated - Clinical trials for Chronic Venous Insufficiency

Radiofrequency Ablation vs. Laser Ablation of the Incompetent Small Saphenous Vein

Start date: September 2008
Phase: Phase 4
Study type: Interventional

The aim of this study is to perform a randomized, prospective trial comparing the two current methods of treatment for chronic venous insufficiency related to the Small Saphenous Vein (SSV) to evaluate complications and outcomes for each method, and ultimately, to see if one is superior to the other.

NCT ID: NCT02248701 Terminated - Clinical trials for Spinal Cord Injuries

Testosterone Plus Finasteride Treatment After Spinal Cord Injury

Start date: April 27, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether testosterone plus finasteride treatment will improve musculoskeletal health, neuromuscular function, body composition, and metabolic health in hypogonadal men who have experienced ambulatory dysfunction subsequent to incomplete spinal cord injury. The investigators hypothesize that this treatment will improve bone mineral density, enhance muscle size and muscle function, and improve body composition, without causing prostate enlargement.