Ventilation Therapy

6

Review clinical trials related to Ventilation Therapy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Initiation of Noninvasive Ventilation in ALS Patients With Chronic Respiratory Insufficiency

This research will study whether noninvasive ventilation (NIV) used to treat chronic respiratory insufficiency in patients with amyotrophic lateral sclerosis (ALS) can be initiated as successfully in the outpatient setting as in the conventional inpatient setting, and what the costs of these alternative initiation methods are.

Participants needed: 120
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Tampere UniversityUpdated: Jan 27, 2026Locations: 1
Eligibility criteria

ALS diagnosed by a neurology and [+1]

impaired cognition to give informed consent to participation [+3]

Status: Not yet recruiting

Impact of Home Non Invasive Ventilation in Patients With Chronic Obstructive Pulmonary Disease Discharged From Assiut University Hospital

This study aims to evaluate the impact of long-term home non-invasive ventilation (NIV) on patients with COPD

Participants needed: 40
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Sep 30, 2025
Eligibility criteria

Patients more than 18 year old. [+2]

Other significant respiratory disorders (e.g,history suggestive OSA, Body Mass I... [+7]

Status: Recruiting

PEEP vs. ZEEP in Out-of-Hospital-Cardiac-Arrest

Out-of-hospital cardiac arrest (OHCA) remains a major cause of mortality, with low survival probabilities to hospital discharge. Despite the frequent use of airway management and mechanical ventilation during resuscitation, there is limited evidence regarding the optimal ventilation strategy to improve oxygen delivery and patient outcomes. The present study aims to investigate the effects of positive-end-expiratory-pressure (PEEP) set at 5 mbar compared to zero-end-expiratory-pressure (ZEEP) on the return of spontaneous-circulation (ROSC) in adult patients with OHCA.

Participants needed: 600
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Muehlenkreiskliniken, MKKUpdated: Aug 6, 2025Locations: 3
Eligibility criteria

Adults >= 18 years [+2]

Patients < 18 years, [+2]

Status: Not yet recruiting

Early Mobilisation and Relational Touch Practice on Intubated Patients of Intensive Care Unit

41.3% of patients hospitalized in intensive care express feeling anxiety when they are systematically questioned. Ventilatory weaning is one of the moments of anxiety for the patient. While being conscious he must tolerate invasive ventilation. The early mobilization of patients in intensive care must be started early, within 24-48 hours, after the patient wakes up. Early mobilization is part of the weaning process from invasive mechanical ventilation in intensive care. It is recommended to reduce it to use relaxation therapies. Several studies have assessed the impact of relational touch in conscious or unconscious patients in intensive care. The SRLF consensus conference in 2010 recommends the use of massage for anxiolytic purposes. This study aims to assess the impact of relational touch versus standard care on anxiety during the first bedside session, in intubated intensive care patients ventilated for at least 48 hours and presenting with RASS (Richmond agitation sedation scale). ) from 0 to -1. The study will aussi assess the impact of relational touch versus standard care on the following patient parameters: * Evaluation of caregiver anxiety with the Spielberger inventory before and after the session * Increasing the duration of the bedside session; * Variations in pain, assessed by the Behavioral Pain Scale (BPS) at the end of the session; * The level of agitation/vigilance at the beginning and at the end of the session with the Richmond agitation-sedation scale (RASS); * Induced variations in blood pressure; * Induced variations in oxygen saturation; * The variations induced on the respiratory rate; * The variations induced on the heart rate; * The need to prescribe psychotropic drugs on the day of the first bedside; * Reduction in the number of days of invasive mechanical ventilation between the first bedside session and discharge from intensive care unit (maximum D28 after the first bedside session). This is a national, multicenter, cluster, randomized, controlled trial with 4-stage stepped-wedge design (1:1:1:1 randomization), phase III, superiority, open-label, comparing systematic practice relational touch by the paramedical team during bedside sessions, versus standard care (without relational touch). The benefit is above all for the patient with a better experience of bedside sessions and a reduction in ventilation time, therefore bed rest, leading to a reduction in decubitus complications. The expected economic benefit involves the reduction of decubitus complications and therefore their cost and the reduction of hospitalization times in intensive care.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Apr 6, 2025Locations: 1
Eligibility criteria

Patient needing help from another person to mobilizing [+11]

Status: Not yet recruiting

High Flow Nasal Cannula for Stabilization of Extremely Premature Infants

A prospective observational study evaluates the safety and efficacy of using High-Flow Nasal Cannula to stabilize extremely preterm infants immediately after birth. Following placental transfusion, high flow nasal cannula at 6-8 l/min is administered along with intermittent tactile stimulation. Criteria for switching to other interventions like continuous positive airway pressure or positive pressure ventilation are set for cases of persistent bradycardia or low Saturation of oxygen (SpO2).

Participants needed: 60
Trial details
Age: 0-2Biological sex: AllType: InterventionalSponsor: Charles University, Czech RepublicUpdated: Nov 14, 2024Locations: 1
Eligibility criteria

Preterm infants born between 25+0 and 27+6 gestational weeks [+1]

Previable rupture of membranes, [+2]

Status: Not yet recruiting

Cerebral Blood Flow: Helmet vs Oronasal Mask During Continuous Positive Airway Pressure Ventilation

In this trial the investigators will evaluate blood flow in common carotid artery of healthy subjects treated with Continuous Positive Airway Pressure (CPAP) Ventilation, comparing two different devices: oronasal mask versus Helmet. The hypothesis is that Helmet CPAP reduces carotid flow compared to oronasal mask.

Participants needed: 19
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Papa Giovanni XXIII HospitalUpdated: Jun 28, 2024Locations: 1
Eligibility criteria

Age ≥ 18 years, [+1]

known cardiac pathologies [+4]