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NCT02158923 · ClinicalTrials.gov registry record · NA
Individualized Perioperative Open Lung Ventilatory Strategy
A NA study of Moderated-high Risk of Postoperative Pulmonary Complication and Abdominal Surgery Expected More Than Two Hours, sponsored by Fundación para la Investigación del Hospital Clínico de Valencia.
- Completed
- Registry status
- NA
- Development phase
- 920
- Enrollment target
- 7
- Study locations
NCT02158923 is a NA study of Moderated-high Risk of Postoperative Pulmonary Complication and Abdominal Surgery Expected More Than Two Hours that has completed, run by Fundación para la Investigación del Hospital Clínico de Valencia. The registered enrollment target is 920 participants. The trial reports 7 study locations across 6 states.
The verdict
NCT02158923, a NA study of Moderated-high Risk of Postoperative Pulmonary Complication and Abdominal Surgery Expected More Than Two Hours, has completed, sponsored by Fundación para la Investigación del Hospital Clínico de Valencia.
- COMPLETED
- Registry status
- NA
- Development phase
- 920 participants
- Enrollment target
- 7
- Study locations
Study Summary
The purpose of this study is to determine whether individualized ventilatory management combining the use of low tidal volumes, alveolar recruitment maneuvers, individually titrated positive end-expiratory pressure and postoperative individualized ventilatory support will decrease postoperative complications, unplanned ICU readmissions, ICU and hospital length of stay and mortality compared to a standardized Lung Protective Ventilation (LPV) for all patients at risk.
Conditions Studied
Interventions
- PROCEDURE Alveolar recruitment maneuver
- PROCEDURE Calculation of optimal PEEP
- PROCEDURE Postoperative CPAP
Study Locations (7)
Barcelona
- Hospital Germans Trias i Pujol - Badalona
- Hospital de la Santa Creu i Sant Pau - Barcelona
Massachusetts
- Massachusetts General Hospital - Boston
Buenos Aires
- Hospital Privado de la Comunidad - Mar del Plata
Madrid
- Hospital Gregorio Marañón - Madrid
Valencia
- Department of Anesthesia and Critical Care; Hospital Clinico Universitario - Valencia
Uppland
- Uppsala University Hospital - Uppsala
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 920 participants |
| Start Date | 2014-09 |
| Est. Completion | 2016-04 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02158923
The ClinicalTrials.gov registry entry for NCT02158923 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 920 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Fundación para la Investigación del Hospital Clínico de Valencia, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Moderated-high Risk of Postoperative Pulmonary Complication appearing as the primary indexed condition, and to 3 interventions - of which Alveolar recruitment maneuver is the first listed.
NCT02158923 reports 7 study locations spanning 6 distinct geographic areas - top geographies include Barcelona, Massachusetts, Buenos Aires.
Frequently Asked Questions
What is clinical trial NCT02158923 about?
NCT02158923 is a clinical study titled "Individualized Perioperative Open Lung Ventilatory Strategy". The purpose of this study is to determine whether individualized ventilatory management combining the use of low tidal volumes, alveolar recruitment maneuvers, individually titrated positive end-expiratory pressure and postoperative individualized ventilatory support will decrease postoperative comp...
What is the current status of trial NCT02158923?
This trial is currently completed. It is a NA study. The enrollment target is 920 participants. The study started on 2014-09. Estimated completion is 2016-04.
What conditions does trial NCT02158923 study?
This clinical trial studies the following conditions: Moderated-high Risk of Postoperative Pulmonary Complication, Abdominal Surgery Expected More Than Two Hours.
What interventions are being tested in trial NCT02158923?
The interventions under investigation include: Alveolar recruitment maneuver (PROCEDURE), Calculation of optimal PEEP (PROCEDURE), Postoperative CPAP (PROCEDURE).
Who is sponsoring clinical trial NCT02158923?
This trial is sponsored by Fundación para la Investigación del Hospital Clínico de Valencia, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02158923 being conducted?
This trial has 7 study locations across Massachusetts, Buenos Aires, Barcelona, Madrid, Valencia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Moderated-high Risk of Postoperative Pulmonary Complication
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Abdominal Surgery Expected More Than Two Hours
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