Understanding reverse trigger in patients on mechanical ventilation
Official title: Incidence of Reverse Trigger Phenotypes and Response to Ventilatory Adjustments in Patients With ARDS
Run by Hospital Civil de Guadalajara · NCT06148467 · Data updated 2026-11-12
This study looks at how often patients with severe lung problems on mechanical ventilation experience a condition called reverse trigger, to see how it affects their treatment and recovery.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 90 Years |
| Sex | All |
| Enrollment | 130 (estimated) |
| Sponsor | Hospital Civil de Guadalajara Academic / other |
| Locations | 1 site (Guadalajara) |
| Status | Recruiting |
| Started | November 17, 2023 |
| Main results expected | December 31, 2027 |
| Study ends | February 1, 2028 |
| Registry record updated | September 16, 2026 |
| Trial ID | NCT06148467 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults diagnosed with ARDS who are currently on mechanical ventilation.
✕Probably not a fit
Patients under 18 years old, those with tracheostomy status, pneumothorax, or tube thoracostomy with air leaks may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to determine the incidence of reverse trigger (RT) in patients with acute respiratory distress syndrome (ARDS) who are receiving mechanical ventilation. Participants will be monitored continuously using esophageal manometry to detect RT and assess their response to ventilatory adjustments. Data will be collected on various clinical parameters, including ventilator settings and patient outcomes, to better understand the dynamics of RT in this population. The study will involve trained investigators who will analyze ventilator waveforms and other metrics to characterize RT events.
Why it matters
Potential benefit: If successful, this study could improve the management of mechanically ventilated patients with ARDS by identifying and addressing reverse trigger events.
How similar studies have gone: While the specific approach of this study may be novel, similar studies have explored mechanical ventilation dynamics and their impact on patient outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of ARDS according to the Berlin criteria and added New Global Definition 2023 * Mechanical ventilation Exclusion Criteria: * \<18 years * Tracheostomy status * Pneumothorax * Tube thoracostomy with air leaks
Where it's running
-
Hospital Civil Fray Antonio Alcalde
Guadalajara, Mexico Recruiting
Study contacts
- Principal investigator: Miguel Ibarra Estrada, MD — Hospital Civil Fray Antonio Alcalde
- Study coordinator: Miguel Ibarra-Estrada, MD
- Email: drmiguelibarra@hotmail.com
- Phone: +523317593502
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Effect of expiratory time constant (RCexp) on lung ventilation and blood flow in ventilated ARDS patients
This tests whether the expiratory time constant (RCexp) changes how air and blood are distributed in the lungs of adults with ARDS who are on mechanical ventilation.
-
Observing physiological changes in ARDS patients in the prone position
This study looks at how lying on the stomach affects breathing and oxygen levels in patients with Acute Respiratory Distress Syndrome to see if it can help improve their recovery.
-
Pulse Wave vs Saline Bolus EIT to measure lung perfusion in ARDS
This study tests whether pulse wave EIT or saline bolus EIT can best show lung blood flow in ARDS patients on mechanical ventilation.
-
Computed inspiratory muscle pressure to monitor inspiratory effort during pressure-targeted assist/control ventilation
This study tests a noninvasive computed pressure method (cPmus) to see if it matches the traditional esophageal pressure method for measuring inspiratory effort in adults on pressure-targeted ventilation with spontaneous breathing.
-
Noninvasive estimate of inspiratory effort to monitor pressure support ventilation
This study tests whether a noninvasive computed inspiratory muscle pressure (cPmus) can match the traditional esophageal pressure method for adults on pressure support ventilation.
-
Driving pressure-guided individualized PEEP vs standard PEEP during upper abdominal surgery
In this randomized trial, adults at higher risk of breathing problems after upper abdominal surgery will try a personalized PEEP level based on the lowest driving pressure and compare it to a fixed PEEP of 5 cmH2O to see if it lowers postoperative lung complications.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.