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Weaning clinical trials

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NCT ID: NCT06009731 Recruiting - Clinical trials for Mechanical Ventilation

Diaphragmatic Speckle Tracking During Spontaneous Breathing Trial

DIAST
Start date: June 12, 2023
Phase:
Study type: Observational

Currently, measurement of transdiaphragmatic pressure (Pdi) using oesophageal and gastric balloons is the gold standard for the assessment of diaphragmatic effort. This technique is relatively invasive and its interpretation may be complex. The diaphragmatic longitudinal strain (LSdi) and strain rate (LSRdi) might provide additional information in the assessment of diaphragmatic effort and movement during SBT, allowing early detection of diaphragmatic dysfunction. Patients will be monitored during a 30-120 minutes SBT consisting of no assistance on the ventilator using CPAP with a pressure level of 0 cmH2O. Parameters to evaluate diaphragm function will include diaphragmatic strain (LSdi and LSRdi), diaphragmatic thickening fraction (TFdi), and airway occlusion pressure (ΔP0.1 and ΔPocc). These parameters will be measured immediately before ('baseline') the SBT, as well as 2 minutes ('early' assessment), 15 ('intermediate' assessment) and 30 minutes ('late' assessment) after the beginning of the SBT.

NCT ID: NCT05719194 Recruiting - Clinical trials for Mechanical Ventilation

Effect of a Personalized Weaning Strategy on Weaning Success

P-Wean
Start date: March 14, 2023
Phase: N/A
Study type: Interventional

Weaning from mechanical ventilation is a daily challenge in intensive care units, as it can take up to 50% of the total duration of ventilation. The longer the duration of ventilation is, the more there is complication related with it. Even when the spontaneous breathing trial is succeeded, 10 to 20% of extubations are failed and requires re-intubation. There is two different ways to assess if the patient is capable of breathing by its own : T-piece which can be considered as hard to succeed (it can delay extubation for some patients) or pressure support ventilation with no PEEP which can be too easy and lead to an extubation too early. Studies have identified risk factors of weaning induced pulmonary oedema wich is one of the main cause of failed extubation (up to 60%). The purpose of P-WEAN is to evaluate whether a personalized strategy for weaning from mechanical ventilation, including daily search for weaning criteria and individualization of the weaning modality (T-piece or pressure support ventilation with zero PEEP) based on the existence of WIPO risk factors (obesity, COPD, cardiopathy) improves weaning success compared with usual practice.

NCT ID: NCT05629819 Recruiting - Clinical trials for Mechanical Ventilation

Effect of Early Non-invasive Phrenic Nerve Stimulation on Weaning in Mechanically Ventilated Patients

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

the early application of non-invasive PNS in MV patients can increase the number of days without mechanical ventilation, delay disuse phrenic atrophy, and improve the strength of inspiratory muscle.

NCT ID: NCT05260853 Recruiting - Weaning Clinical Trials

Early Detection and Early Intervention Program in High-risk Patients to Avoid Invasive Long-term Ventilation

PRiVENT
Start date: August 1, 2021
Phase: N/A
Study type: Interventional

Early prediction and prevention of prolonged weaning in high risk patients via identification through a computer model and additional assistance in treatment through certified weaning centers in Baden-Württemberg

NCT ID: NCT04602182 Recruiting - Clinical trials for Respiration, Artificial

Effectiveness of Musicotherapy in Weaning From Mechanical Ventilation

Start date: October 19, 2020
Phase: N/A
Study type: Interventional

1. OBJECTIVES: General objective: Assess the effects of a music therapy intervention during the weaning from the mechanical ventilation in a group of patients, and compare it to the usual clinical practice. Specific objectives: Main objective: assess the effect of a music therapy intervention on the length of the weaning in a group of critical patients, and compare it to a group of critical patients who receive the usual clinical practice. Secondary objectives: - Compare the levels of sedo-analgesia required in critical patients receiving the music therapy intervention during the process of weaning versus the levels of sedo-analgesia required by the control group. - Compare the Anxiety-agitation level in critical patients receiving the music therapy intervention during the process of weaning, versus the anxiety-agitation leved felt by the control group. - Compare the level of pain in critical patients receiving the music therapy intervention during the weaning versus the level of the pain felt by the control group. - Compare the level of delirium in critical patients receiving music therapy during the weaning versus the level of delirium of the control group. - Compare heart and breath frequency, blood pressure and oxygen saturation in critical patients receiving music therapy during the mechanical ventilation extubation (weaning) process, versus the index of control group. - Compare the stress perceived in critical patients receiving music therapy intervention during the mechanical extubation process, versus the level of the control group, which receives the usual medical care (without intervention with music therapy), 90 days after Inico of the process, Perceived the Stress Scale (PSS). - Describe and analyze the experience by the patient of the intervention with music therapy the weaning process and the coping strategies possible for musicotherapeutic intervention, using a Semi-instructed interview that takes place at 90 days beginning the process. 2. DESIGN: single blind clinical trial in parallel groups, single blind clinical trial. 3. POPULATION of this study are patients who initiate weaning for ventilation mechanics.

NCT ID: NCT03929328 Recruiting - Clinical trials for Mechanical Ventilation

Effect of High Flow Oxygen Therapy in Spontaneous Breathing Trial on Weaning in Mechanical Ventilated Patients

HOST
Start date: June 17, 2019
Phase: N/A
Study type: Interventional

This clinical trial is aimed to show a spontaneous breathing trial using high flow oxygen therapy may lower weaning failure rate and reintubation rate than using T-piece.

NCT ID: NCT02487927 Recruiting - Clinical trials for Mechanical Ventilation

The Classification of Difficult Weaning and the Predictive Value of Relative Factors for Difficult Weaning

Start date: June 2012
Phase: N/A
Study type: Observational

To evaluate the distribution of different types of difficult weaning and the predictive value of weaning relative factors.

NCT ID: NCT01135121 Recruiting - Weaning Clinical Trials

Role of Diaphragm Fatigue in Weaning From Mechanical Ventilation

Start date: May 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether the diaphragm develops contractile fatigue during a weaning trial and if this is associated with weaning failure.