Trial · NCT07896967
Impact of Inspiratory Effort and Patient-Ventilator Interaction During the Transition Phase
NCT07896967, Not yet recruiting, Pontificia Universidad Catolica de Chile
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Impact of Inspiratory Effort and Patient-Ventilator Interaction During the Transition Phase. Trials, record NCT07896967. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896967
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Impact of Inspiratory Effort and Patient-Ventilator Interaction During the Transition Phase
- NCT number
- NCT07896967
- Status
- Not yet recruiting
- Enrollment
- 250 participants, estimated
- Lead sponsor
- Pontificia Universidad Catolica de Chile
- Conditions
- Mechanically Ventilated Patients, Acute Respiratory Failure (ARF)
- Interventions
- PVA classification software
- First posted
- 2026-10-27
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Successful liberation from mechanical ventilation within 28 days of enrollment | 28 days | Defined as the time from entry into the transition phase (study enrollment) to the first episode of sustained extubation, lasting at least 7 days |
| Secondary | Ventilator free days (at day 28) | 28 days | Number of ventilator free days at day 28 |
| Secondary | ICU length of stay (28 days) | 28 days | Length of ICU stay, measured in days from enrollment |
| Secondary | ICU length of stay (at day 90) | 90 days | ICU length of stay, measured in days from enrollment |
| Secondary | Mortality at day 28 | 28 days | Mortality at day 28 |
| Secondary | Mortality at day 90 | 90 days | Mortality at day 90 |
| Secondary | Incidence of weaning failure or reintubation | 7 days | reintubation within 7 days after extubation. |
| Secondary | Rate of complications | 28 days | including tracheostomy and resumption of sedatives |
| Secondary | Physiological characterization | 7 days | based on different inspiratory effort levels (ΔPocc) |
| Secondary | Incidence (AI) of patient-ventilator asynchrony | 7 days | Number of asynchronous respiratory cycles, expressed as a proportion of the total respiratory cycles recorded, overall and by PVA type. |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07896967
GET https://conductscience.org/api/trials/v1/NCT07896967/registered