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NCT ID: NCT02837601 Not yet recruiting - Shoulder Pain Clinical Trials

Pneumoperitoneum Management With SurgiQuest AirSeal® at Low vs. Higher Pressure

PRESSURE
Start date: March 2021
Phase: N/A
Study type: Interventional

A prospective, randomized, controlled single-center clinical Study designed to evaluate Physician Preference related to the use of the SurgiQuest AirSeal® Insufflation System (AIS) at low vs. higher pressures for the Management of pneumoperitoneum. Subjects will be randomized in a 1:1 treatment device to control ratio into one of two (2) different study arms: 1. AIS with an insufflation pressure target of 9mmHg ±1mmHg; or 2. AIS with an insufflation pressure target of 15mmHg ±1mmHg.

NCT ID: NCT02832505 Not yet recruiting - Clinical trials for Chronic Kidney Disease

Applications of MRI in Kidney Disease

Start date: October 30, 2024
Phase:
Study type: Observational

This study has two major purposes: 1. To test developed multiple anatomic and functional MRI methods; 2. To evaluate the potentials of these MRI methods in the diagnosis, prognosis, and monitoring of the progression of renal dysfunction. These purposes will be achieved by performing pilot studies with cohorts of patients.

NCT ID: NCT02809235 Not yet recruiting - Asthma Clinical Trials

Fatty Acids in Airway Smooth Muscle of Asthmatics

Start date: October 2023
Phase: N/A
Study type: Interventional

In this proof of concept study, the investigators aim to determine if supplementation with coconut oil causes an increase in cholecystokinin and cholecystokinin receptor expression in the airway smooth muscle of lean asthmatics, and whether these changes correlate with changes in airway stiffness (estimated by bronchodilator reversibility, airway reactivity, and airway resistance) or symptom control. The investigators propose a 5 week, single center trial in 20 lean patients with mild asthma (not taking inhaled corticosteroids) aged 18 and older. Subjects will supplement their usual diets with 3 tablespoons of coconut oil, a commercially available oil with high dodecanoic acid content, for 3 weeks. To quantify changes in airway smooth muscle cholecystokinin and cholecystokinin-receptor expression, each subject will undergo bronchoscopy with endobronchial biopsies before and after coconut oil ingestion. For the secondary analysis, subjects will also complete spirometry with bronchodilator testing, methacholine challenge, body plethysmography, and an Asthma Control Questionnaire (ACQ) before and after the dietary intervention. This information will be used to compare the changes in airway smooth muscle cholecystokinin and cholecystokinin receptor expression to changes in bronchodilator reversibility, airway reactivity, airway resistance, and symptom control. In the exploratory aims, the investigators will correlate the changes in airway smooth muscle cholecystokinin and cholecystokinin receptor expression with changes in FEV1 and peak flow measurements. The investigators therefore hope to elucidate information about the mechanistic role of cholecystokinin in airway smooth muscle stiffness and contraction.

NCT ID: NCT02805985 Not yet recruiting - Clinical trials for Degenerative Disc Disease

Post-market Surveillance Study of FLXfit™ TLIF Interbody Fusion Device

FLXFit
Start date: October 2016
Phase: N/A
Study type: Interventional

This study is a post-market clinical follow-up study. A post-market, prospective clinical trial will be conducted. The data collected from this study will serve the purpose of confirming safety and performance of the FLXfit™ implant.

NCT ID: NCT02795923 Not yet recruiting - Lung Cancer Clinical Trials

Nivolumab Alone or in Combination With Decitabine/Tetrahydrouridine in Non-small Cell Lung Cancer

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

The purpose of this study is to assess whether treatment with the study drug tetrahydrouridine-decitabine (THU-Dec) in combination with nivolumab is more effective than treatment with nivolumab alone in patients with NSCLC. Decitabine is an investigational (experimental) drug that works by depleting DNA methyltransferase 1 (DNMT1). DNMT1 is an enzyme, or protein that causes chemical changes, often increased in cancer. Blocking DNMT1 has been shown to reduce tumor formation. Decitabine is experimental in this study because it is not approved by the Food and Drug Administration (FDA) for patients with lung cancer. Decitabine is approved by the FDA for treating patients with a blood disease called myelodysplastic syndrome (MDS, a condition where the bone marrow does not make blood cells normally). THU is an investigational (experimental) drug that works by blocking an enzyme that breaks down decitabine. This enzyme is highly expressed in solid tissues of the body, limiting the distribution of decitabine into these tissues, including solid cancer tissues. So, THU will increase the time cells in your body are exposed to decitabine. The idea is that THU will also increase the time that the lung cancer cells are exposed to decitabine. THU is experimental because it is also not approved by the FDA, although it has been extensively used in clinical trials, including several cancer trials.

NCT ID: NCT02783079 Not yet recruiting - Insomnia Clinical Trials

Insomnia Interventions in Cancer Survivors

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

This study looks at two different interventions used for the treatment of insomnia in survivors of breast, colon, lung, prostate and gynecologic cancer.

NCT ID: NCT02779192 Not yet recruiting - Clinical trials for Noise Induced Hearing Loss

A Phase 2b Study of SPI-1005 to Prevent Acute Noise Induced Hearing Loss

PANIHL
Start date: November 2018
Phase: Phase 2
Study type: Interventional

SPI-1005 is a novel oral drug that contains a glutathione peroxidase mimetic (ebselen) that will be tested in subjects with a history of NIHL at risk for additional NIHL. The goal of this multi-center Phase 2b study is to determine whether SPI-1005 is effective in reducing an acute NIHL in this affected population. In this Phase 2b study subjects with prior NIHL will be enrolled and exposed to a calibrated sound challenge (CSC) that induces a slight acute NIHL.

NCT ID: NCT02755571 Not yet recruiting - Clinical trials for Stage IVA Colon Cancer

Financial Impact Assessment Tool in Patients With Metastatic Colorectal Cancer

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

This clinical trial studies the use of the financial impact assessment tool in patients with colorectal cancer that has spread from the primary site to other places in the body. Gathering information about patients with colorectal cancer over time may help doctors better understand the financial impact of cancer and help patients avoid financial problems during treatment.

NCT ID: NCT02741804 Not yet recruiting - Clinical trials for Mild Cognitive Impairment

Lifestyle Intervention Program for Cognitive Impairment

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

The purpose of the Lifestyle Intervention Study is to investigate the influence of a micronutrient supplement in combination with a comprehensive lifestyle intervention program on retinal amyloid, among patients with Mild Cognitive Impairment (MCI). Patients will be placed on supplement or placebo throughout their 18-month study participation. Patients will also be given lifestyle training on nutrition, physical activity, cognitive and social activity, meditation and sleep, which have all been proven to positively affect cognition over time. Throughout their participation, patients' cognitive functioning will be monitored with comprehensive imaging, neuropsychological testing, blood testing and study compliance.

NCT ID: NCT02740933 Not yet recruiting - Brain Tumor Clinical Trials

Demeclocycline Fluorescence for Intraoperative Delineation Brain Tumors

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

This research study is studying a drug called Demeclocycline that may help brain surgeons see tumors with a microscope during surgery.