A Real World Study of Respiratory Critical Disease.

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Acute Respiratory Distress Syndrome (ARDS) is a form of acute diffuse lung injury caused by various etiologies, which rapidly progresses to acute respiratory failure. It is characterized by a sudden onset and severe clinical course. Globally, ARDS affects approximately 3 million individuals each year, accounting for about 10% of admissions to intensive care units (ICUs). Due to the lack of specific pharmacological therapies, mechanical ventilation remains the mainstay of treatment. Therefore, identifying and analyzing prognostic factors for ARDS patients is of great significance for improving patient outcomes and reducing the incidence of poor prognosis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with underlying diseases associated with high risk of ARDS, including but not limited to: sepsis, pneumonia, multiple trauma, pulmonary contusion, inhalation injury, massive blood transfusion, other high-risk conditions, or other factors causing excessive respiratory drive.

• Patients meeting the inclusion criteria for a high-risk ARDS population.

• Patients (or legal representatives) who have provided a signed and dated informed consent form.

Locations
Other Locations
China
Fudan University, Zhong Shan Hospital
RECRUITING
Shanghai
Contact Information
Primary
Yuxian Wang, Doctor
wang.yuxian@zs-hospital.sh.cn
86-13482359545
Time Frame
Start Date: 2019-03-01
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 500
Sponsors
Leads: Ming Zhong

This content was sourced from clinicaltrials.gov