Clinical Trials Logo

Filter by:
NCT ID: NCT03584958 Enrolling by invitation - Glaucoma Clinical Trials

Comparing Refractive and Visual Outcomes of MIGS and Traditional Surgeries

Start date: August 1, 2018
Phase:
Study type: Observational

The primary goal of this study is to evaluate refractive and visual outcomes in glaucoma patients who will be having either traditional glaucoma surgery or minimally invasive glaucoma surgery, also known as MIGS.

NCT ID: NCT03642093 Enrolling by invitation - Pancreatic Cancer Clinical Trials

HOPE - A Study to Evaluate the Effect of a Prehabilitation Program on GI Cancer Patients Planning to Undergo Surgery

HOPE
Start date: August 1, 2018
Phase: Phase 4
Study type: Interventional

A one-group prospective cohort study design with measures collected pre- and post-intervention. The primary goal of this study is to evaluate the effect of a multimodal prehabilitation preoperative program on changes in frailty in upper gastrointestinal surgical oncology patients.

NCT ID: NCT03662828 Enrolling by invitation - Kaposi's Disease Clinical Trials

Epidemiological Description of the Kaposi's Disease in France's Southeast

KAPOSI-1
Start date: August 1, 2018
Phase:
Study type: Observational

The purpose of this study is to evaluate the prevalence of the Kaposi's disease in France's southeast on 10 years (from 2007 to 2017)

NCT ID: NCT03927599 Enrolling by invitation - Solid Tumor, Adult Clinical Trials

Advanced Refractory Solid Tumors With TP53 Mutations Register Study

Start date: August 1, 2018
Phase:
Study type: Observational

The efficacy and safety of the PARP inhibitor in combination with the VEGFR inhibitor will be investigated in advanced refractory solid tumors patients with TP53 mutation .

NCT ID: NCT06361524 Enrolling by invitation - Clinical trials for Heart Failure With Reduced Ejection Fraction

Gut Microbiome Profiling in Patients With Chronic Heart Failure

Start date: August 1, 2018
Phase:
Study type: Observational

The goal of this observational study is to learn about the composition and function of the gut microbiome in adults with chronic heart failure with reduced ejection fraction. The main questions the study aims to answer are: 1. How does the gut microbiome and its interactions with the host change over time in adults with chronic heart failure? 2. How do these changes relate to heart failure disease severity and complications?

NCT ID: NCT03433157 Enrolling by invitation - Dental Caries Clinical Trials

Assessment of Stainless Stain Crowns Placed Using the Hall Technique and Traditional Technique

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate and compare the clinical performance of Stainless Stain Crowns Placed Using the Hall Technique and Traditional Technique

NCT ID: NCT03851406 Enrolling by invitation - Airway Inflammation Clinical Trials

Woodsmoke Particulate + Hypertonic Saline

Smokeysal
Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Deployment of military personnel has been associated with increased respiratory illness likely due, in part, to inhalation of unusual particulate matter (PM), such as from burn pits. Inflammation is a key initial response to inhaled particulates. The investigator has developed a protocol using inhaled wood smoke particles (WSP) as a way to study PM-induced airway inflammation. Exposure to wood smoke particles causes symptoms, even in healthy people, such as eye irritation, cough, shortness of breath, and increased mucous production. The purpose of this research study is to see if a single treatment of inhaled hypertonic saline (HS) can diminish this PM-induced airway inflammation by rapidly clearing the WSP inhaled particles from airway surfaces. The exposure will be 500 ug/m³ of WSP for 2 hours, with intermittent exercise on a bicycle and rest. The wood is burned in a typical wood stove and piped into the chamber.

NCT ID: NCT03992599 Enrolling by invitation - Clinical trials for Adenocarcinoma of the Colon

Prospective Study of Oncologic Outcomes After Laparoscopic Modified Complete Mesocolic Excision for Non-metastatic Right Colon Cancer [PIONEER Study]

Start date: August 1, 2019
Phase:
Study type: Observational [Patient Registry]

This study is a multi-institutional, prospective, observational study evaluation oncologic outcomes of laparoscopic modified complete mesocolic excision (mCME) on right-sided colon cancer. The primary outcome of this study is 3 year disease-free survival. Secondary outcome measures include 3 year overall survival, incidence of surgical complications, completeness of mCME, and distribution of metastatic lymph nodes.

NCT ID: NCT03995342 Enrolling by invitation - Frailty Syndrome Clinical Trials

The Correlation and Intervention of Intestinal Flora and Frailty in the Elderly

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The study aim to evaluate the improvement and correlation of soluble dietary fiber (prebiotics) in the frailty of elderly people by a randomized, double-blind, placebo-controlled clinical trial.

NCT ID: NCT04026477 Enrolling by invitation - Behavior Clinical Trials

Evaluation of Link for Equity (School Staff Population)

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The investigators propose to develop and evaluate Link for Equity, a trauma-informed system of care. Link, a system of support for ACE-affected children, is composed of universal school Trauma-Informed Care. Preventing Racism through Awareness and Action (PRAA) is a perspective-taking racism/discrimination prevention intervention for school staff that increases awareness of racism and how it impacts students and promotes empathy for students of color. Link for Equity will be translated to be culturally responsive for 12 secondary public schools in metropolitan and rural Minnesota with substantial racial/ethnic minority students and racial/ethnic disparities in school discipline and violence. Using a nested, rigorous, and ethically acceptable randomized waitlist control design, the investigators will implement and evaluate Link for Equity sequentially for two years in each school. The overall goal is to evaluate if Link for Equity can reduce school violence disparities.