The Effect of Ciprofol on Breathing Patterns, Respiratory Drive, and Inspiratory Effort in Mechanically Ventilated Patients

  • STATUS
    Recruiting
  • participants needed
    20
  • sponsor
    Capital Medical University
Updated on 29 February 2024

Summary

Sedatives and analgesics are usually given for analgesic, anxiolytic, or sedating purposes for patients with critical illness, while they inevitably inhibit respiratory and circulatory function. Sometimes, patients receive deep sedation to induce hypoventilation or suppress spontaneous respiratory effort. The sedation level in clinical practice is usually assessed with subjective sedation scoring systems, such as the Richmond Agitation Sedation Scale (RASS). However, studies have found that sedation depth based on RASS is not a reliable marker of respiratory drive during critical illness. In recent years, researchers have proposed to monitor the effects of sedatives and analgesics on respiratory indicators and to implement lung-protective sedation, such as P0.1, Pocc, Pmus, WOB, and PTP. However, different pharmacological characteristics, different depths of sedation, and different sedation regimens among different sedatives and analgesics make a great difference in their effects on respiration. Ciprofol is an analog of propofol, with increased stereoselective effects adding to its anesthetic properties, is increasingly used in the intensive care unit, but its effects on respiration are not well understood. Therefore, this study aims to investigate the effects of ciprofol on respiratory patterns, respiratory drive, and inspiratory effort in mechanically ventilated patients.

Details
Condition Mechanical Ventilation, Sedation and Analgesia
Age 18years or above
Treatment Ciprofol
Clinical Study IdentifierNCT06287138
SponsorCapital Medical University
Last Modified on29 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

The patient received surgery under general anesthesia and admitted into the ICU
The patient has been intubated and is receiving invasively mechanically ventilated with the mode of pressure support (PSV) or continuous positive airway pressure (CPAP)
The patient requires sedative medication targeting RASS -2 to +1 for comfort, safety and to facilitate the delivery of life support measures

Exclusion Criteria

Age < 18 years
Body mass index (BMI) <18 or >30 kg/m2
Pregnancy or lactation
Brain stem tumors, myasthenia gravis, or neuromuscular diseases
Acute severe neurological disorder and any other condition interfering with RASS assessment
Systolic blood pressure < 90 mmHg after appropriate intravenous volume replacement and continuous infusions of 2 vasopressors
Heart rate < 50 beats per minute or second- or third-degree heart block in the absence of a pacemaker
Contraindicate or allergic to any of the study medications
Acute hepatitis or serious hepatic dysfunction (Child-Pugh class C)
Chronic kidney disease with glomerular filtration rate (GFR) < 60 ml/min/1.73m2
Alcohol abuse
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