Non-invasive Phrenic Nerve Stimulation in ARDS Patient
Recruiting now · Not applicable
Conditions studied: ARDS, Human, Ventilator-Induced Lung Injury, Diaphragm Injury
In brief
Reduced diaphragmatic activity during mechanical ventilation can lead to diaphragmatic disuse atrophy, atelectasis, increased lung stress and strain, and hemodynamic impairment. This, in turn, may prolong the duration of mechanical ventilation, make weaning more difficult, and even increase mortality. Synchronizing phrenic nerve stimulation to promote diaphragmatic activity may prevent ventilator-induced lung injury and ventilator-induced diaphragm dysfunction, thereby improving patient outcomes. Surgically implanted phrenic nerve stimulation has been used in certain neurological disorders, but the effects of percutaneous non-invasive synchronized phrenic nerve stimulation in patients with ARDS undergoing mechanical ventilation remain unclear and require further investigation.
Key facts
- Study ID
- NCT06572280
- Run by
- Southeast University, China
- People needed
- 10
- Starts
- 2024-08-01
- Expected to finish
- 2025-01-30
- Last updated by the study team
- 2024-08-27
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult ARDS patients undergoing controlled mechanical ventilation
- The duration of endotracheal intubation < 48 hrs
You may not qualify if…
- Neurological condition affecting motor neuron or muscle (e.g. ALS)
- Paralysis of the phrenic nerve
- Proven or suspected spinal cord injury
- Conditions that limit diaphragm movement
- Patients with Implanted cardiac support systems (pacemaker, implanted defibrillator)
- Patients with implanted medical pumps
- Pregnancy
- Patients with skin lesions, infections or strictures in throat/neck area
- Patients with metallic implants
- Refusal to sign informed consent
Where it is running
- Zhongda Hospital, School of Medicine, Southeast University — Nanjing, Jiangsu, China (enrolling)
Full record on ClinicalTrials.gov
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