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PreVent - surface electromyography in intensive care to assess respiratory effort and describe patient-ventilator interaction

PreVent - surface electromyography in intensive care to assess respiratory effort and describe patient-ventilator interaction - PreVent

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00040745
Enrollment
40
Registered
2026-06-29
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensive care patients on mechanical ventilation, including those requiring prolonged ventilation and weaning from mechanical ventilation.

Interventions

Group 1: Prospective observational study of adult critically ill patients on mechanical ventilation who are experiencing difficult weaning or severe acute respiratory distress syndrome (ARDS). As part

Sponsors

Universitätsklinikum Erlangen – Anästhesiologische Klinik
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Either a group requiring postoperative ventilation for >24 hours: a patient receiving postoperative ventilation or a patient with an expected ventilation duration of >24 hours Or patients with severe ARDS: Severe ARDS according to the Berlin definition (respiratory failure not due to cardiac failure or volume overload, acute onset, bilateral opacities, paO2/FiO2 <100) - Nasogastric esophageal pressure probe in place - Admission to a participating intensive care unit

Exclusion criteria

Exclusion criteria: - Pre-existing severe lung disease - Previous participation in this clinical trial (PreVent) - Exclusion from the trial based on a healthcare directive - Poor prognosis (death expected within the next few hours despite maximum therapy) - Pregnancy - The patient is institutionalized by court or administrative order

Design outcomes

Primary

MeasureTime frame
Subjective assessment of respiratory effort and patient-ventilator asynchrony by intensive care staff before and after presentation of the sEMG data. The assessment is conducted using a study-specific questionnaire during the early phase of spontaneous breathing and at the start of intermittent weaning.

Secondary

MeasureTime frame
System usability (System Usability Scale, SUS) and descriptive analysis of patient-ventilator asynchronies and potential surrogate parameters.

Countries

Germany

Contacts

Public ContactRoland C. E. Francis

Universitätsklinikum Erlangen – Anästhesiologische Klinik

direktion.an@UK-Erlangen.de+49 9131 85-33677

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026