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Respiratory clinical trials

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NCT ID: NCT06044402 Not yet recruiting - Oxygenation Clinical Trials

Different Tidal Volume on Oxygenation, Respiratory Mechanics, and Pulmonary Complications in Older Patients Undergoing Trendelenburg Pneumoperitoneum Surgery

Start date: October 8, 2023
Phase: N/A
Study type: Interventional

The investigators want to assess the effect of intraoperative low tidal volume vs intermediate tidal volume on respiratory mechanics, oxygenation and pulmonary complications in older patients undergoing Trendelenburg pneumoperitoneum surgery.

NCT ID: NCT05867082 Completed - Neck Pain Clinical Trials

Effects of Neural Mobilization on Respiratory Parameters in Chronic Neck Pain

Start date: April 30, 2021
Phase: N/A
Study type: Interventional

Objective: Neural mobilization (NM) is commonly used to treat nerve disorders, and it is useful for disorders associated with neck and arm pain. This study aimed to determine the effects of NM on respiratory function in patients with chronic neck pain. Methods: Overall, 26 patients with neck pain were randomly assigned to two groups: NM or control. In these participants, respiratory function and active cervical range of motion were assessed before and after intervention. Furthermore, the participants were provided a visual analog scale (VAS) and Fremantle Neck Awareness Questionnaire (FreNAQ). Each participant underwent 15 treatment sessions (5 days per week for 3 weeks). Further, in the NM group, in addition to conventional treatment, 10 sessions of neural mobilization were performed.

NCT ID: NCT05657626 Completed - Respiratory Clinical Trials

Effect of Active Period Length of Firefighters on Respiratory and Climbing

Start date: December 25, 2022
Phase:
Study type: Observational

The goal of this observational cross-sectional study is to examine the effect of the active period of firefighters in the units on respiratory functions and stair climbing performance. In the relevant fire department, aged between 18 and 64, who do not have a psychological, cognitive or emotional problem, a chronic heart or lung disease that would prevent them from participating who have been active for at least two years, will be included. The main questions it aims to answer are: - What is the effect of the active period of firefighters on respiratory functions? - What is the relationship between the length of active period of firefighters in the profession and their stair climbing performance? Participants sociodemographic characteristics will be questioned by using the Demographic Data Form. - Pulmonary function test and respiratory muscle strength measurement will be performed with the Pony Fx pulmonary function test device. - The Cornell Musculoskeletal Disorders Questionnaire will be used to evaluate musculoskeletal disorders. - The 6 Minute Walk Test will be performed to evaluate exercise capacity. - Stair Climbing Test will be applied to evaluate stair climbing performance.

NCT ID: NCT05268263 Completed - Lung Clinical Trials

Feasibility of AI-based Classification of Normal, Wheeze and Crackle Sounds From Stethoscope in Clinical Settings

Start date: January 6, 2022
Phase: N/A
Study type: Interventional

Assessing the feasibility and testing the accuracy of the developed artificial intelligence algorithms for detection of wheezes and crackles in patients with lung pathologies in clinical settings on unseen local patient data acquired through three digital stethoscopes.

NCT ID: NCT04342702 Active, not recruiting - COVID-19 Clinical Trials

A Study on the Prospective Cohort Library of COVID-19 in Southeran

Start date: March 16, 2020
Phase:
Study type: Observational

This is a multi-centre population-based follow-up study for all 504 patients with laboratory-confirmed COVID-19. This study establishes a standardized and structured clinical database to provide complete and multidimensional clinical diagnosis and treatment data of novel coronavirus pneumonia, which also support future epidemiological, infectious disease study and patients' prognosis, by collecting clinical data and the related data of patients with novel coronavirus pneumonia in Southern Zhejiang province.

NCT ID: NCT04219644 Completed - Respiratory Clinical Trials

Evaluation of the "Breatheasy" in Pre-hospital Care

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

In the emergency department, a sick child is usually seen first by the nursing staff. Their job is to quickly assess how sick the child is and what immediate care is needed. The nurse will usually use suitable devices to check vital signs, such as body temperature, pulse rate and blood oxygen levels. However, normally the respiratory rate has to be manually counted (this is the average number of breaths taken each minute) because there is no suitable device which can automatically do this assessment. To overcome this problem we have produced a noncontact device that can automatically measure respiratory rate in children. The device has been designed using the latest technology and works by directly sensing the air coming from the nose or the mouth when held at about 20 cm from the face. It has been tested on adults and children and compared to the usual methods of measuring respiratory rate. We have used comments and Suggestions from members of the public and healthcare professionals from hospital, general practice and the ambulance service to help us develop the device. With this study, we explore the applicability and usefulness of the device in a range of difference clinical and nonclinical settings. Its performance will be carefully evaluated on children and adults in children's nurseries, schools, university, hospital emergency departments, general practice surgeries and ambulances. In the future, when using the device nursing staff will easily be able to measure each child's respiratory rate so that the most seriously ill children will be identified earlier and get correct treatment more quickly. This will ensure that the right children get admitted to intensive care units sooner and, in some cases, deaths will be prevented.

NCT ID: NCT00515840 Completed - Asthma Clinical Trials

GPIAG and Leicester Asthma and Dysfunctional Breathing (GLAD) Study: a Randomised Controlled Study

GLAD
Start date: October 2003
Phase: Phase 3
Study type: Interventional

Breathing retraining supervised by a physiotherapist will result in improvements in the quality of life and asthma control of patients treated for asthma in the community with symptoms suggestive of dysfunctional breathing. To investigate the effects of breathing retraining on clinical and physiological parameters of asthma control, to identify the characteristics of patients who benefit, to perform a health economic evaluation.