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Healthy Volunteers clinical trials

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NCT ID: NCT02872688 Completed - Healthy Volunteers Clinical Trials

Influence of GanedenBC30 (Bacillus Coagulans GBI-30, 6086) on the Gut Microbiome in Healthy Adults

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

The purpose of this study is to investigate the effect of a GanedenBC30, a probiotic bacteria (Bacillus coagulans strain GBI-30, 6086), on the gut microbiome in healthy adults. Subjects will complete a 2-week run-in period prior to receiving GanedenBC30. The study is open-label and subjects will act as their own controls as the microbiome is unique to individuals. During the run-in period, subjects will collect two stool samples and complete daily bowel habit diaries in order to understand usual habits and profile the microbiome for each subject. 30 subjects will take part in this research study conducted at Nutrasource Diagnostics Inc. Subjects will take GanedenBC30 for four weeks. Stool samples will be collected at the end of the study and daily bowel habit diaries maintained for the duration of the study.

NCT ID: NCT02871648 Completed - Healthy Volunteers Clinical Trials

The Role of Minerelocorticoid Receptor on Modulating Aldosterone Production

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

The purpose of this research protocol is to determine if the same effects are observed in vivo in humans using a similar approach. Demonstrating that mineralocorticoid acts on zona glomerulosa cells to regulate aldosterone production in a short feedback loop would provide important insight into hormone regulation, and explain variability in pathophysiologic states such as hypertension and cardiovascular diseases.

NCT ID: NCT02870400 Completed - Healthy Volunteers Clinical Trials

A Study to Examine the Safety and Tolerability of Single Ascending Doses of REGN2477

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

The primary objective of the study is to assess the safety and tolerability of single ascending doses of REGN2477 in healthy women not of childbearing potential.

NCT ID: NCT02869893 Completed - Healthy Volunteers Clinical Trials

MRCP: A Reliable, Non Invasive Method for Staging Chronic Pancreatitis in Pediatrics

Start date: August 10, 2016
Phase: N/A
Study type: Interventional

The goal of this research study is to learn more about the pancreas. The investigators want to use Magnetic Resonance Cholangiopancreatography (MRCP) to learn more about the size of a normal pancreas. MRCP is a special kind of MRI exam that produces detailed images of the pancreas. The investigators also want to figure out how much fluid the pancreas releases in response to secretin. Secretin is a chemical in the body that causes the pancreas to release fluid that helps with digestion. Secretin is used during the MRCP (MR-PFT) to help identify dysfunction of the pancreas. MR elastography (MRE) will be used to measure how hard the pancreas is. MRE is a special kind of MRI that uses vibrations to image tissue.

NCT ID: NCT02867098 Completed - Healthy Volunteers Clinical Trials

XmAb5871 Bioavailability Study

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

An open label comparison of concentration of the study medication administered intravenously (IV) versus subcutaneously (SC) in healthy volunteers.

NCT ID: NCT02864264 Terminated - Healthy Volunteers Clinical Trials

Single Ascending Dose and Multiple Ascending Dose Study in Healthy Participants and Proof of Mechanism Study in Patients With Ulcerative Colitis

Start date: September 14, 2016
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to determine if single and multiple doses of BMS-986184 are safe and well tolerated in healthy male and female subjects. The primary purpose of the proof of mechanism study is to determine safety and efficacy in patients with ulcerative colitis.

NCT ID: NCT02860975 Active, not recruiting - Healthy Volunteers Clinical Trials

Prolonged Hypoxic Breathing in Healthy Volunteers: a Safety Study

MGH-nitrogen
Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to define the safety and the biochemical-physiological response of prolonged exposure to a normobaric low-oxygen environment in healthy volunteers.

NCT ID: NCT02858973 Completed - Healthy Volunteers Clinical Trials

A Dose-Escalation Study to Evaluate Safety, Tolerability and Pharmacokinetics of Multiple Doses of Q203 in Normal Healthy Male and Female Volunteers

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

This is randomized, double-blind, placebo-controlled, multiple ascending dose study of Q203 in healthy volunteers conducted at one study center in the United States

NCT ID: NCT02858752 Recruiting - Healthy Volunteers Clinical Trials

Memory and Attention in Healthy Children

MASK
Start date: October 6, 2016
Phase: N/A
Study type: Interventional

This project studies memory and attention in healthy children aged from 5 to 17 years. The processes investigated are short term memory (auditory and visual) and attention. To characterize these processes involved in childhood, neuropsychological and neurophysiological assessments will be performed (using Electro-encephalography measures, behavioural responses and questionnaires).

NCT ID: NCT02856633 Completed - Hypertension Clinical Trials

Preliminary Testing of the Vitaliti CVSM Wearable, Vitaliti Spirotoscope, and Vitaliti IVD Station

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

The study objective is to satisfy the testing requirements for the Qualcomm Tricorder XPRIZE Competition. This requires an oversight model using the Vitaliti CVSM Wearable, Vitaliti Spirotoscope, and Vitaliti IVD Station to continuously monitor the patient's five core vital signs and to detect the health conditions required by the competition.