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NCT ID: NCT04505059 Recruiting - Anesthesia Clinical Trials

Different Anesthetic Strategies on Postoperative Cognitive Function and Delirium in Patients Undergoing Cardiac Surgery

Start date: September 11, 2020
Phase: N/A
Study type: Interventional

This is a prospective, multi-center, double-blind, randomized clinical trials.

NCT ID: NCT03964675 Completed - Condition Clinical Trials

Evaluation of SenseGuard™- a Noninvasive Respiratory Rate Measuring Device

Start date: January 13, 2019
Phase: N/A
Study type: Interventional

The SenseGuard™ is a new respiratory rate measuring and logging non-invasive device, and measures the respiratory rate by responding to changes in air moisture content in exhaled air. A prospective single-center, single arm study, designed to assess the bias, accuracy , precision and safety of the SenseGuard™ device in measuring of respiratory rate in adult patients. The study shall include a single invitational visit with a respiratory rate measurement duration of 30 minutes for each of 25 adult subjects hospitalized in internal wards.Subjects will be invited to participate should they meet all of the eligibility criteria. Following informed consent, subjects will be measured with both Microstream capnograph and SenseGuard™ measuring simultaneously so their results can be compared.

NCT ID: NCT03427762 Completed - Healthy Clinical Trials

Compare the Effects of Agility and Cycling Exercise Training on Mobility and Balance in PD and Healthy Old Adults

Start date: February 3, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to compare the effectiveness and specificity of agility and cycling exercise training on balance and mobility outcomes in PD and age and gender matched healthy controls. The hypothesis is that due to being profoundly deconditioned, agility and cycling will be similarly effective in PD but agility will be more effective then cycling in healthy old adults, in improving mobility and balance.

NCT ID: NCT03393598 Recruiting - Graft Loss Clinical Trials

Recipient Site Pre-conditioning in Fat Grafting

Start date: January 8, 2018
Phase: N/A
Study type: Interventional

This study aims to investigate the preparation of the recipient site prior to autologous fat grafting (AFG) using different methods.

NCT ID: NCT03274674 Completed - Blood Clot Clinical Trials

Use of Injectable-platelet-rich-fibrin (I-PRF) to Thicken Gingival Phenotype

Start date: April 4, 2017
Phase: N/A
Study type: Interventional

The main objective of this study is to investigate whether the for individuals with thin gingival thickness who are susceptible to gingival recession, the investigators will use i-PRF with microneedle to increase gingival thickness without the need for surgical procedures

NCT ID: NCT02450006 Recruiting - Condition Clinical Trials

Intermountain INSPIRE Registry

Start date: April 2015
Study type: Observational [Patient Registry]

To collect biological samples, clinical information and laboratory data from patients diagnosed with any healthcare-related conditions who are seen at facilities affiliated with Intermountain Healthcare, including patients and their family members, and to collect the same information and samples from a general population including disease-free subjects.

NCT ID: NCT01722136 Completed - Condition Clinical Trials

"We Walk": Impact of Exercise Dose on Health Outcomes Among Women Ages 60-75

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

The overall goal is to determine whether any energy expenditure compensation in response to 16 weeks of aerobic exercise at a higher-dose is greater compared to a lower-dose intervention in older women, and to begin to investigate underlying physiological mechanisms that influence energy expenditure changes in older women.