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NCT ID: NCT02697279 Terminated - Clinical trials for Abscess of Skin and/or Subcutaneous Tissue

Loop Drainage: Effectiveness in Treating Cutaneous Abscesses

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

In the Emergency Department (ED), patients frequently seek medical treatment for cutaneous abscesses. Traditional incision and drainage (I&D), with or without packing of cutaneous abscesses has long been the accepted standard of care. This procedure is often very painful for the patient. Additionally, compliance with wound care and follow-up can present barriers to proper care and healing. Research has suggested that incision and loop drainage of an abscess may be another effective treatment for simple cutaneous abscess. Thus far, research into this procedure has been limited to the pediatric population with small sample sizes. In these previous studies, this technique was found to be an effective and less painful treatment for abscesses. Research has not been done in the adult population using this procedure. If this procedure is found to be as effective and less painful in the adult population, then it should be considered as a potential preferred I&D method for cutaneous abscess in the ED.

NCT ID: NCT02697136 Terminated - Clinical trials for Familial Hypoalphalipoproteinemia

CER-001 Therapy as a Novel Approach to Treat Genetic Orphan Diseases

TANGO
Start date: December 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the impact of 29 intravenous infusions of CER-001 vs. placebo, given at weekly (9 infusions) and biweekly (20 infusions) intervals on carotid vessel wall area as measured by 3TMRI, when administered to patients with familial primary hypoalphalipoproteinemia with proven CVD and appropriate background lipid-lowering therapy.

NCT ID: NCT02696759 Terminated - Breast Cancer Clinical Trials

Gut Microbiome & Gastrointestinal Toxicities as Determinants of Response to Neoadjuvant Chemo for Advanced Breast Cancer

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

The purpose of this research is to test whether bacteria that normally live in the intestines play a role in fighting cancer. It is believed that the development and behavior of these immune cells may be influenced by bacteria and other microorganisms living in the gut. In turn, the activities of these immune cells could work with anti-cancer therapies to make them more, or less, effective.

NCT ID: NCT02696291 Terminated - Viral Infection Clinical Trials

Safety and Pharmacokinetics of UV-4B Solution Administered Orally as Multiple Ascending Doses to Healthy Subjects

Start date: May 27, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and pharmacokinetics of UV-4B oral solution when administered to healthy subjects three times a day (TID) for 7 days.

NCT ID: NCT02696278 Terminated - Obesity Clinical Trials

Hummus for Health: Dietary Quality and Health Outcomes in Toddlers

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

The goal of this study is to examine the effect of increasing children's intake of fiber and unsaturated fat, through daily servings of hummus and vegetables, on their microbiome profile.

NCT ID: NCT02696226 Terminated - Clinical trials for Aortic Valve Disorder

Frequency of Reduced Leaflet Motion After Surgical Aortic Valve Replacement and Transcatheter Aortic Valve Replacement.

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

This is a prospective, randomized pilot study in patients undergoing Sugical Aortic Valve Replacement (SAVR) and Transcatheter Aortic Valve Replacement (TAVR) to estimate the incidence of reduced leaflet motion and assess the impact of perioperative anticoagulation on the incidence of reduced leaflet motion.

NCT ID: NCT02695680 Terminated - Lung Cancer Clinical Trials

Lung SBRT Motion Management (GCC 1619)

Start date: October 27, 2017
Phase:
Study type: Observational

Real-time optical surface monitoring data will be acquired from 44 human patients with primary or metastatic lung lesions during and after their 4DCT scan (standard-of-care at our institution). A patient-specific 4D model will be developed using the raw 4DCT projections time-correlated with real-time surface monitoring. In addition, before delivering each dose fraction (3 - 5 for lung SBRT), we will acquire three 15s kV fluoroscopic image acquisitions, time-correlated with optical surface monitoring. The acquisitions will be distributed over three well-spaced beam angles, e.g., every 4th angle for a 12-field plan.

NCT ID: NCT02695667 Terminated - Clinical trials for Obstructive Sleep Apnea

Quantitative Genioglossal Muscle Strength in Obstructive Sleep Apnea (OSAS)

EatonOSAS
Start date: February 2016
Phase:
Study type: Observational [Patient Registry]

Quantitative Genioglossal muscle strength in Obstructive Sleep Apnea (OSAS) defined in the clinical spectrum of subjects with Snoring Disturbance, Oral Appliance Therapy Responsive, and CPAP Responsive

NCT ID: NCT02695602 Terminated - Nasal Obstruction Clinical Trials

Trial Comparing Microdebrider-Assisted Inferior Turbinoplasty (MAIT) vs Submucous Resection (SMR)

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

This is a prospective, patient blinded, randomized, clinical trial enrolling patients with symptoms and signs of nasal obstruction related to enlarged inferior turbinates. The purpose of this study is to compare two different surgical methods, both of which are already in common use, for the treatment of nasal obstruction in patients with inferior turbinate hypertrophy.

NCT ID: NCT02695290 Terminated - Clinical trials for Carcinoma, Non-Small-Cell Lung

Afatinib in EGFR+NSCLC (Recurrent or Stage IV) - Patients With Poor Performance Status (ECOG 2 or 3)

Start date: March 17, 2016
Phase: Phase 4
Study type: Interventional

There is a medical need for improving treatment of poor performance status patients with EGFR driver mutations and documenting safety and tolerability of existing agents.