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NCT ID: NCT03871543 Completed - Visual Acuity Clinical Trials

Late Night Study 2: End-of-Day Assessment of Asymptomatic and Symptomatic Soft Lens Wearers

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

This is a 2-Part, 8-Visit, single-center, open-label, bilateral and dispensing clinical study. In Part 1 (Visits 1-4) all subjects will be Test Lens 1, in Part 2 (Visits 1-4) eligible subjects will be dispensed Test Lens 2 based on their responses to the CLDEQ-8 questionnaire. Subjects scoring between 11 and 19 on the CLDEQ will not continue into Part 2

NCT ID: NCT03871621 Completed - Clinical trials for Type 2 Diabetes Mellitus

Left Ventricular Functional Changes of Uncontrolled Diabetes by Dapagliflozin Treatment Trial

ELUCIDATE
Start date: April 1, 2019
Phase: Phase 4
Study type: Interventional

The primary purpose of this study is to evaluate the efficacy of the SGLT2 inhibitor dapagliflozin, as compared with standard care of diabetes, on left ventricular (LV) structural and functional change in asymptomatic type 2 diabetes mellitus (DM) patient.

NCT ID: NCT03871790 Completed - Pancreatic Cancer Clinical Trials

Peptide-based Immunization for Colon- and and Pancreas-carcinoma

PICOP-GLOBAL
Start date: April 1, 2019
Phase:
Study type: Observational

An international, multicenter study to identify tumor molecular particularities and neoepitopes among participants with colorectal and pancreatic tumors undergoing surgery.

NCT ID: NCT03872258 Completed - Healthy Clinical Trials

Effectiveness of an Intensive Intervention to Improve Physical Activity in Postmenopausal and Sedentary Women

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

This is a randomized clinical trial aimed at postmenopausal women aged 45 to 70 years old selected in urban primary care centers of two centers (Spain). Its objective is to evaluate the effects of an intensive intervention in the increase of physical activity and the decrease of sedentary lifestyle in postmenopausal and sedentary women.

NCT ID: NCT03872414 Completed - Parkinson Disease Clinical Trials

Emotion Study/Substudy: Flexible Brain Study

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

The proposed research applies the highly innovative technology of real-time functional Magnetic Resonance Imaging (rtfMRI) to examine plasticity of brain-regulatory mechanisms related to cognitive and affective processing and to determine benefits for cognition and affect in young and older adults and in Parkinson Disease (PD) patients.

NCT ID: NCT03872674 Completed - Clinical trials for Patients Undergoing Endoscopic Retrograde Cholangiopancreatography in Prone Position

A Trial Comparing High-flow Nasal Oxygen With Standard Management for Conscious Sedation During Endoscopic Retrograde Cholangiopancreatography in Prone Position

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

Traditional conscious sedation for endoscopic retrograde cholangiopancreatography in prone position places patients at risk of desaturation, and high-flow nasal oxygen may reduce the risk. The aim of this study is to evaluate the role of high-flow nasal oxygen during endoscopic retrograde cholangiopancreatography. The investigators will compare the lowest SpO2 of standard nasal oxygen cannula group and that of high-flow humidified oxygen-delivery system group during the procedure.

NCT ID: NCT03873766 Completed - Empyema, Pleural Clinical Trials

Management of Pleural Space Infections

Start date: April 1, 2019
Phase: Phase 4
Study type: Interventional

Currently, there is no high-quality evidence comparing the clinical outcomes and cost effectiveness of surgical drainage combined with antibiotics versus dual-agent intrapleural fibrinolytic therapy (IPFT) catheter drainage of pleural space infections with concomitant antibiotic therapy. The absence of comparative data is a challenge for surgical and medical services in clinical decision-making for this common and morbid condition. This is a pilot study comparing surgical drainage of the pleural space in complex pleural effusions to bedside chest tube drainage using dual agent IPFT with the intent to inform on study algorithm and endpoint performance in anticipation of a multi-institutional randomized clinical trial.

NCT ID: NCT03873844 Completed - Clinical trials for Cognitive Impairment

Improving Thinking in Everyday Life: Pilot Study A

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

This is a pilot study at the University of Alabama at Birmingham. The purpose of this initial study is to test how effective a new therapy is for improving participants ability to think, particularly how rapidly they process information that they receive from their senses, e.g., sight, hearing,… . The study will also test whether the new therapy improves how often and how well they are able to carry out tasks that rely on thinking in their daily life. The therapy will combine a computer game that ask participants to identify targets on the screen as rapidly as possible with a set of psychological techniques that will help to apply the improvements that are made in how rapidly participants process information as a result of the game to carrying out tasks that rely on thinking in your daily life.

NCT ID: NCT03876171 Completed - Problem Behavior Clinical Trials

Culturally Modified Family Based Therapy for Haitian Youth in South Florida

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

The CIFFTA study is a unique intervention that will develop and implement a culturally-specific, family-based individual, drug use, sexual risk and delinquency risk reduction program for Haitian youth ages 13-17 in Miami-Dade County, Florida.

NCT ID: NCT03877341 Completed - Lumbar Spine Fusion Clinical Trials

Sagittal Parameters After Mono Segmental Lumber Fusion: Interbody Versus Postrolateral Fusion

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

To compare postoperative radiographic sagittal parameters after monosegmental lumbar fusion: posterior lumbar interbody fusion versus postrolateral fusion in treatment of lumbar spine instability