Percutaneous Temporary Placement of a Transvenous Phrenic Nerve Stimulator for Diaphragm Pacing U… (NCT03659552) | Clinical Trial Compass
CompletedNot Applicable
Percutaneous Temporary Placement of a Transvenous Phrenic Nerve Stimulator for Diaphragm Pacing Using Jugular Access
Paraguay13 participantsStarted 2018-05-07
Plain-language summary
Study conducted to confirm phrenic nerve stimulation using the a transvenous Phrenic Nerve Stimulator in the left jugular vein.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* 18 years of age or older;
* Able and willing to give informed consent or whose legally authorized representative is able and willing to give informed consent;
* Able to undergo general anesthesia (sedation, intubation, and mechanical ventilation);
* Acceptable indication for atrial septal defect closure.
Exclusion Criteria:
* Subject has an ejection fraction of \< 30%
* Subject has a co-morbid illness or life expectancy \< 2 years
* Subject has experienced an acute myocardial infarction within 72 hours prior to this procedure
* Subject is contraindicated for or unwilling to take aspirin or anticoagulants
* Subject is in cardiogenic shock
* Subject has other cardiovascular disease requiring open heart surgery
* Subject is known to have a demonstrated intra cardiac thrombus on echocardiography
* Subject has been treated with paralytic medications within 72 hours prior to procedure
* Subject has significant thoracic abnormalities such that placement of a left subclavian line would be difficult
* Inability to cannulate the left subclavian vein (post-consent exclusion)
* Subject has a known or suspected phrenic nerve paralysis
* Subject has co-existing temporary or implanted cardiac electrical devices such as a pacemaker or defibrillator
* Subject has an active systemic infection or local infection at or around the insertion site
* Subject is known or suspected to be pregnant or is lactating
* Subject will be unavailable for, or is unwilling to comply with…
What they're measuring
1
Successful insertion of the LIVE Catheter into the left jugular vein and stimulation of phrenic nerves
Timeframe: through study completion, an average of 14 days