Pneumonia Clinical Trials

Find Pneumonia Clinical Trials Near You

The Application of Different Sedation Protocols in ICU Patients With Severe Pneumonia

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

This study collected data from 600 patients with severe pneumonia to compare the duration of mechanical ventilation under different sedation regimens in real-world settings. It also evaluated and compared the sedation success rates, hemodynamic changes, and clinical outcomes of patients with severe pneumonia.

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

∙ (1)From February 1, 2023, to March 30, 2024, diagnosed with severe pneumonia in the Respiratory Intensive Care Unit of Xiangya Hospital, Central South University. The diagnosis of severe pneumonia is based on meeting at least one major criterion or three or more minor criteria:

• Major criteria:

• ①Infectious shock requiring vasopressor therapy despite adequate fluid resuscitation;②Respiratory failure requiring tracheal intubation or mechanical ventilation.

• Minor criteria:

⁃ Respiratory rate ≥ 30 breaths/min; ②Oxygenation index (PaO2/FiO2) ≤ 250;

‣ Involvement of multiple lobes; ④Altered mental status and/or disorientation; ⑤Blood urea nitrogen ≥ 20 mg/dl (7.14 mmol/L); ⑥Systolic blood pressure \< 90 mmHg requiring aggressive fluid resuscitation. (2)Patients receiving mechanical ventilation who require sedation treatment. (3)Age ≥ 18 years.

Locations
Other Locations
China
Xiangya Hospital Central South University
RECRUITING
Changsha
Contact Information
Primary
Yuanyuan Li, Doctor
Leeround@csu.edu.cn
13975806790
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 600
Treatments
Use cyclopofol group
Initially use propofol as the sedative medication, with a continuous usage duration of more than 48 hours.
Control group
Initially use non-propofol sedative medications, with a continuous usage duration of more than 48 hours.
Related Therapeutic Areas
Sponsors
Leads: Xiangya Hospital of Central South University

This content was sourced from clinicaltrials.gov