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Environmental Exposure clinical trials

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NCT ID: NCT04028791 Completed - Clinical trials for Environmental Exposure

Sickle Cell Trait and Exercise, Effect of Hot Environment

TDex
Start date: September 25, 2017
Phase: N/A
Study type: Interventional

The heterozygous form of sickle cell disease is clinically asymptomatic. Nevertheless, it was observed that, the sickle cell trait is associated with serious medical complications especially during intense physical efforts. Moreover, the exposure to a hot environment (tropical climate) is suspected to be a determining factor in the occurrence of these medical complications. However, the relationship between sickle cell trait and death during effort is not well established. Furthermore, the cascade of events that usually cause sickle cell crisis such as red blood cells sickling and rhabdomyolysis and which affect microcirculation are not known. Our main objective in this study is to verify whether young healthy active men with sickle cell trait have reactive hyperemia to their hemoglobinemic condition during exercise; to identify the contribution of hot environment on these possible disturbances; and to determine underlying mechanisms. In addition, disturbances in the regulation of glucose metabolism in healthy subjects under hot environment have been reported, marked by a significant increase in postprandial blood glucose. Therefore, this project is also intended to assess the contribution of the disturbance of glycoregulation during exercise under hot environment in active sickle cell trait carriers. The imbalance of pro and anti oxidant agents, the adhesion and inflammation markers will also be evaluated. Results of this study will allow a better understanding of physio-pathological mechanisms leading to vascular accidents during exercise under tropical climate in young healthy sickle cell trait carriers; and to identify physical activity programs and nutritional interventions adapted to patients with sickle cell disease under hot environment.

NCT ID: NCT03802721 Completed - Clinical trials for Environmental Exposure

Pharmacokinetics of Benzo[a]Pyrene: Impact of Diet

Start date: January 24, 2019
Phase: Early Phase 1
Study type: Interventional

Evaluation of the pharmacokinetics for [14C]-benzo[a]pyrene ([14C]-BaP) and metabolites in plasma and urine over 48 hours following a 50 ng dose (5.4 nCi) alone, following 7 days' consumption of Brussels sprouts, and following 7 days' consumption of a supplement containing 3,3'-diindolylmethane (DIM).

NCT ID: NCT03631667 Completed - Clinical trials for Environmental Exposure

Ultralow Dose PAH Binary Mixture Study

Start date: October 1, 2018
Phase: Early Phase 1
Study type: Interventional

Evaluation of the pharmacokinetics for [14C]-benzo[a]pyrene ([14C]-BaP) and metabolites in plasma and urine over 48 hours following a 50 ng dose (5.4 nCi) alone or with 1250 ng phenanthrene.

NCT ID: NCT03558698 Completed - Sleep Clinical Trials

Are Cognition and Sleep Affected by Exposure to Carbon Dioxide and Bio Effluents During Sleep?

Start date: January 23, 2018
Phase: N/A
Study type: Interventional

The aim of the project is to examine whether children's sleep and cognition are affected by exposure to CO2 and other bio effluents during sleep. The participants of the study are 36 children recruited from local schools in Aarhus, Denmark. The study takes place in the climate chambers at the Department of Public Health, Aarhus University. These chambers allow for experimental testing on humans with advanced exposure generation while avoiding contamination from other sources and controlling temperature, humidity, noise, odor, and light. The children will be sleeping in the chambers under three different conditions: - One night of good ventilation with a CO2 level of maximum 800 ppm - One night of good ventilation with high levels of CO2 (3,000 ppm) - One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents. The study is a within-group design, and groups of six children will be sleeping in the chambers for three nights (separated by seven days). The different groups of children are exposed to the conditions in a randomized order. The study is double-blinded (of security reasons the persons responsible for CO2 concentrations in the chambers are not blinded). The study takes place on schools nights. The children arrive at 6 pm and leave for school the morning after. In the evening the children are tested for approximately 30-40 minutes to measure their cognitive performance using CANTAB (Cambridge Neuropsychological Test Automated Battery) on iPads. After completing the test, dinner is served and the children have some spare time before going to bed. During night, the quality of sleep (awake time and different sleep stages) will be monitored using Fitbit devices. Sleep quality will also be evaluated using a short sleep questionnaire. The next morning the cognitive performance of the children will be tested again using CANTAB before the children leave for school. Our primary hypothesis is that children will perform worse on the cognitive test when exposed to high levels of CO2 and other bio effluents than compared to low levels of CO2 and bio effluents in a well-ventilated room. In addition to that our secondary hypotheses are: - Children will perform worse on the cognitive test when exposed to high levels of CO2 and other bio effluents than compared to CO2 alone. - Children will sleep less well in an environment with poor ventilation and high levels of CO2 and other bio effluents compared to sleeping in a well-ventilated room with low levels of CO2. - Children will sleep less well in an environment with poor ventilation and high levels of CO2 and other bio effluents compared to sleeping in a room with high levels of CO2 alone. - Children will sleep less well and perform worse on the cognitive test when exposed to high levels of CO2 compared to low levels of CO2.

NCT ID: NCT03550989 Completed - Clinical trials for Environmental Exposure

Real-Life Passive Exposure Assessment of IQOS

Start date: December 5, 2017
Phase:
Study type: Observational

This study is a non-interventional observational study designed to assess the impact of passive exposure to IQOS environmental tobacco aerosol in Non-Smokers in a real-life restaurant setting.

NCT ID: NCT03444922 Completed - Clinical trials for Environmental Exposure

Effects of BPA on Insulin and Glucose Responses

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

The National Institutes of Health has encouraged research examining effects of BPA, yet evidence in humans evaluating the effects of BPA on insulin and glucose concentrations remains exclusively associative in nature. Thus, the primary purpose of this study is to determine whether an acute oral ingestion of BPA impacts insulin and glucose concentrations, and other endocrine factors (Pro-insulin, C-Peptide, Estrogen, triglycerides). Findings from this pilot study will inform public health recommendations for food packaging and provide much needed experimental evidence as to whether BPA poses any public health risk.

NCT ID: NCT03440307 Completed - Clinical trials for Environmental Exposure

Intervention to Reduce Bisphenol A Exposure in Women

Start date: November 12, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a 3-week intervention reduces urinary Bisphenol A (BPA) in women with obesity

NCT ID: NCT03342209 Completed - Clinical trials for Environmental Exposure

Utility of High Flow Nasal Cannula in CO Toxicity

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

determination of the half-life of COHb in CO-poisoned patients with high flow nasal oxygen therapy in the ED.

NCT ID: NCT03318978 Completed - Clinical trials for Environmental Exposure

Benzo[a]Pyrene Ultralow Dose-Response Study

Start date: April 17, 2018
Phase: Early Phase 1
Study type: Interventional

Evaluation of the pharmacokinetics for [14C]-benzo[a]pyrene ([14C]-BaP) and metabolites in plasma and urine over 48 hours following 4 oral doses of 25, 50, 10 and 250 ng (2.7-27 nCi).

NCT ID: NCT03224455 Completed - Clinical trials for Environmental Exposure

Environmental Assessment of Sleep in Youth

EASY
Start date: January 18, 2018
Phase:
Study type: Observational

In this research study, investigators want to learn more about the factors that influence children's breathing during sleep and their sleep quality. Specifically, investigators are interested in factors that are related to risk of snoring, sleep apnea (a condition where breathing stops during sleep), and poor sleep quality.