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Active clinical trials for "Respiratory Tract (Lung and Bronchial) Diseases"

Results 42671-42680 of 43232

A Multi-center Study to Determine the Prevalence and Influence of Pertussis on Subacute Cough in...

PertussisChronic Cough

A prospective, multi-center, observational clinical trail. Aim to evaluate the real incidence of COPD pertussis and the impact of pertussis on subaute cough.

Unknown status2 enrollment criteria

Doppler Ultrasonographic Assessment of Fetal Internal Thoracic Artery Indexes

Pregnancy RelatedFetal; Circulation

The aim of this study is to assess the feasibility of visualizing the internal thoracic artery (ITA), establishing the normogram for ITA pulsatility index (PI), resistance index (RI) and acceleration/ejection time (AT/ET) at 24-32 weeks.

Unknown status8 enrollment criteria

SARS-CoV-2 (COVID-19) Antibody PrevalencE in an Adult London HIV Cohort

HIV-1-infectionSARS-CoV Infection1 more

Prospective, observational SARS-CoV2 serological surveillance single London HIV outpatient center study using NHS participants

Unknown status5 enrollment criteria

Breathing After COVID-19

GaitCovid191 more

This research; It will be done to perform thoracic movement analysis of young adult individuals who have survived COVID-19 and to compare them with those without a history of COVID-19.

Unknown status5 enrollment criteria

Longitudinal Observational Study for mIddle Term Follow-up Patients Admitted for Acute Dyspnea in...

Longitudinal Observational Study With 6 Months Follow-up

The purpose of the SIDI study is to follow, few months after discharge from the hospital, the patients admitted to the 3 emergency departments in Tunisia for acute dyspnea and to determine the proportion and the factors favoring rehospitalization and death.

Unknown status12 enrollment criteria

Canine COVID-19 Detection Phase 2 and 3

Covid19SARS-CoV2 Infection

The purpose of this study is to determine whether trained medical detection dogs can accurately detect the presence of COVID-19 in people infected with the virus, or using samples of their clothing or body odour. The study will train dogs to identify and discriminate between individuals wearing clothing collected from people infected with SARS-CoV-2 and uninfected individuals under semi-field conditions.Following this training, field testing will be used to determine whether trained dogs can distinguish between people infected with SARS-CoV-2 and uninfected individuals, producing estimates of dogs' sensitivity and specificity.

Unknown status58 enrollment criteria

Evaluation of the Sofia SARS Antigen FIA Assay for COVID-19

SARS-CoV2 Infection

Evaluating the performance of the Sofia SARS Antigen FIA

Unknown status12 enrollment criteria

Immune Response to Seasonal Influenza Vaccination in Multiple Sclerosis Patients Receiving Cladribine...

Multiple SclerosisRelapsing-Remitting1 more

The primary objective of this study is to characterize the antibody response to seasonal influenza vaccine, in patients with active RRMS, treated with cladribine, compared to control individuals with basic immunomodulatory treatment. Serum antibody titers against the respective pathogen will be assessed prior to and 6 to 8 months following vaccination.

Unknown status16 enrollment criteria

Long-term Neurocognitive and Psychiatric Consequences in Severe COVID-19 Survivors.

Covid19Neurocognitive Dysfunction

Long-term neurocognitive and psychiatric consequences of COVID-19 remain mostly unknown to date. It has been reported that coronaviruses cause direct central nervous system infection (Needham et al. 2020). Besides that, new or worsening cognitive impairment commonly occurs and persists in survivors of intensive care unit (ICU) stay (Hosey & Needham. 2020). The purpose of our study is to search and describe the cognitive and psychiatric long-term consequences of COVID-19 on patients who have been discharged from critical care units. This is an ambidirectional cohort study, that attempts to follow adults discharged from critical Care Units Adults due to COVID-19 up to 12 months after discharge, to evaluate the presence of cognitive impairment, linguistic and phonation function, depression, fatigue, functional gastroenterological symptoms, anxiety, or post traumatic disorder, and performance in activities of daily living and physical response to exercise as well.

Unknown status2 enrollment criteria

Cerebral and Renal Oximetry Study in Preterm Patients Who Require Surfactant Administration

Respiratory Distress Syndrome of Prematurity

Respiratory distress syndrome of prematurity (RDSP) is an acute respiratory condition that occurs in preterm infants due to pulmonary surfactant deficiency. Exogenous surfactant administration is a crucial therapeutic measure in the management of RDSP, being the 'less invasive surfactant administration technique' (LISA) the gold standard, according to the latest reviews. Oximetry based on near-infrared spectroscopy is a non-invasive monitoring modality that provides continuous information on the degree of regional hemoglobin saturation present in the underlying tissue, mainly in the venous compartment. It is thus, a reflection of the balance between oxygen supply and demand of oxygen to the tissues. We intend to perform a prospective analysis of newborns under 32 weeks of gestational age who require surfactant administration, as we wish to study cerebral and renal perfusion by oximetry in the group of patients who receive surfactant by LISA and in the group of patients who receive surfactant via endotracheal tube (patients intubated at birth for stabilization), since there are few data published in the literature. Our main hypothesis is that the administration of surfactant by LISA technique does not negatively influence cerebral and renal oximetry. Our secondary hypothesis is that patients requiring intubation at birth will present greater hemodynamic and respiratory instability in the first 72 hours of life, with a greater decrease in cerebral and renal oximetry with the administration of surfactant, compared to the group that does not require intubation at birth.

Unknown status3 enrollment criteria
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