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Normal Subjects clinical trials

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NCT ID: NCT04766138 Completed - Fecal Incontinence Clinical Trials

Trial to Evaluate Fecobionics in Healthy Subjects and Patients

NORMAL
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Fecobionics combines several existing tests to provide novel insight into anorectal function. The purpose for the development was to overcome the technological controversies and disagreement between various tests and unphysiological test conditions. The aim was to imitate defecation as much as possible to the natural process. Fecobionics was developed to simulate stool and to provide the driving pressure and resulting deformations of stool along with a measure of an objective anorectal angle during defecation in a single examination. Fecobionics makes it possible to describe objectively, without disturbing the defecation process, the opening characteristics and pressure signatures during initial entry into the relaxing anal canal. The overall goal is to provide mechanistic understanding of defecation in health and defecatory disorders. It exceeds previous attempts to make artificial stool for evaluation of defecation and integrates other technologies as well. It was designed to have a consistency and deformability of Type 4 (range type 3-5) on the Bristol stool form scale. The range from types 3-5 is found in 70% of healthy subjects. A major novelty is that Fecobionics measures pressures in axial direction; i.e., in the flow direction. It is anticipated that Fecobionics will shed light on the neurophysiology of defecation in health and disease, including understanding the effect of biofeedback and neuromodulatory effect of SNS. It will be of great value to provide endpoints in normal subjects that in future studies can be objective measures for monitoring treatment efficacy. The present protocol is on normal subjects only.

NCT ID: NCT03557450 Completed - Normal Subjects Clinical Trials

A Feasibility Study to Determine PET/CT Imaging of Blood Flow to the Bone

PETCT
Start date: June 11, 2018
Phase: N/A
Study type: Interventional

To evaluate if a commonly used medical bone scan, called positron emission tomography/computed tomography (PET/CT) with sodium fluoride can measure bone blood flow to the hip.

NCT ID: NCT02973334 Completed - Normal Subjects Clinical Trials

Acute Effects of Artificial Sweeteners or Sugar on Hemodynamic and Metabolic Stress Responses

EduStress
Start date: October 2015
Phase: N/A
Study type: Interventional

This exploratory study aims at investigating the acute effects of artificially sweetened and sugar beverage consumption (as compared to water consumption) on acute hemodynamic and metabolic stress response.

NCT ID: NCT02853773 Completed - Normal Subjects Clinical Trials

Effects of Consuming Artificial Sweeteners and Sugar on Cerebral and Physiological Responses

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

This study aims at investigating the acute influence of artificially sweetened beverages consumption (as compared with sugar-sweetened beverages and water consumption) on brain responses to the viewing of food images, on physiological responses (gut-derived hormones and lipid metabolites) and on the food intake behavior.

NCT ID: NCT01889524 Completed - Normal Subjects Clinical Trials

Radioaerossol Pulmonary Deposition Using Mesh in Normal Subjects

Start date: January 2012
Phase: N/A
Study type: Interventional

In vivo deposition studies of aerosol administration during noninvasive ventilation are scarce in the current literature. We assessed 10 normal subjects in a crossover study evaluated by pulmonary scintigraphy aiming to compare radiaoaerosol pulmonary index and radioaerosol mass balance in the different compartments (pulmonary and extrapulmonary) of radiotagged aerosol administered using vibrating mesh nebulizers (VMN) and conventional jet nebulizer (JN) during noninvasive ventilation (NIV).

NCT ID: NCT01801579 Completed - Normal Subjects Clinical Trials

Reproducibility of Ankle Brachial Index After Maximal Exercise

RICATEM
Start date: November 2012
Phase: N/A
Study type: Observational

Hemodynamic changes in the lower limbs are very important and rapid after maximal exercise. The automatic method allows a fastest measurement of the Ankle-Brachial Index (ABI). Thus, it appears important to know whether automatic assessment of ABI is as reliable and reproducible as the manual method.

NCT ID: NCT00220857 Completed - Normal Subjects Clinical Trials

Rabeprazole Protection of Aspirin Induced Gastric Damage.

Start date: September 2005
Phase: Phase 4
Study type: Interventional

To determine the effectiveness of rabeprazole in preventing or decreasing acute gastroduodenal injury caused by therapeutic doses of aspirin in a placebo-controlled, randomized, double-blind parallel group study.