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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04554095
Other study ID # Multimodal Weaning
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 4, 2022
Est. completion date December 1, 2024

Study information

Verified date February 2024
Source Corporacion Parc Tauli
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Weaning from mechanical ventilation (MV) is a complex process in which patients are liberated from the ventilator. Prolongued weaning and weaning failure, defined as the need for reintubation, have different adverse effects, including prolongation of MV, intensive care unit (ICU) and hospital stay, and are also associated with increased incidence of ventilator-associated pneumonia and high mortality. The rate of weaning failure is high, even when the classic extubation criteria are met, so it is necessary to improve scores that allow predicting and determining the ideal time for MV withdrawal. The aim of this study is to design a new multimodal index to predict and optimize weaning results in a personalized way, based on the use and interpretation of data derived from continuous monitoring of critically ill patients. The new multimodal index, in addition to classical respiratory parameters, will include parameters related to patient-ventilator interaction (asynchronies), diaphragmatic function, cardiovascular status and autonomic nervous system function (ANS). The investigators have designed a prospective observational study that will include 126 critical patients from a medical-surgical ICU that meet the classical criteria for weaning. The management of the patients, as well as the weaning process, will be carried out following the usual protocol. In addition to the classical weaning predictor data, data on the patient-ventilator interaction and the function of the autonomic nervous system will be collected by means of specific software (BetterCare). Cardiovascular and diaphragmatic function will be evaluated using ultrasound. Based on the advanced analysis of data from different devices collected throughout the mechanical ventilation period, it will be designed a "personalized" weaning score that should improve the accuracy of the decision-making process and therefore reduce morbidity and mortality. Additional benefits would include lowering health care costs without increasing adverse events.


Recruitment information / eligibility

Status Recruiting
Enrollment 126
Est. completion date December 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with MV> 24 hours. - Patients with orotracheal tube. - Patients who meet the classic criteria of weaning from the MV defined as: Improvement or resolution of the cause required for MV. PaO2> 60mmHg with FiO2=0.4 and PEEP =8cm H2O. Glasgow Coma Score> 10 Temperature <38 ° C. Hemoglobin> 8g / dL No need for vasoactive drugs or at doses <5µg / kg / min Obtaining informed consent. Exclusion Criteria: - Tracheostomy patients. - Patients with neurological pathology with involvement of the brainstem.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Clinical data collection
Respiratory parameters, analytic values, lung ultrasound and echocardiography

Locations

Country Name City State
Spain Candelaria De Haro Sabadell Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Corporacion Parc Tauli

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Multimodal index for weaning prediction evaluation Number of successful weanings evaluated through the new multi-modal index compared to the classic indexes 48 hours after mechanical ventilation withdrawal
Secondary Predictive value of patient-ventilator interaction association between asynchronies and weaning failure From day 1 of mechanical ventilation until 48 hours after mechanical ventilation withdrawal
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