A Protocol Comparing Temporary Transvenous Diaphragm Pacing to Standard of Care for Weaning From Mechanical Ventilation (RESCUE 3)

Lungpacer Medical

Status: Terminated

Conditions: Ventilator Induced Diaphragm Dysfunction

Treatments: Device: Lungpacer Diaphragm Pacing Therapy

Study type: Interventional

Funder types: Industry

Identifiers

NCT03783884

P-300

Details and patient eligibility

About

This clinical investigation is an open-label, multi-center RCT to demonstrate the safety and effective performance of the Lungpacer DPTS (plus standard of care) as compared to Control (standard of care only) in patients aged 18 years or older who are receiving mechanical ventilation. Eligible Subjects will have received mechanical ventilation for ≥96 hours (4 days) and have failed two weaning attempts.

The goal or outcome is to show a numerically greater proportion of subjects weaned in the Treatment (Lungpacer DPTS) group as compared to the Control group.

Full description

The intended patient population is applicable for Lungpacer DPT because there are no noninvasive alternative treatments for patients who are difficult to wean from MV (i.e., ≥96 hours (4 days) on MV) or who have required prolonged MV (>7 days). The intended patient population includes approximately one-third of all patients on mechanical ventilation. Under standard of care, approximately 50% of these patients will recover from mechanical ventilation (Jung, 2016). Standard of care involves daily weaning attempts, known as Spontaneous Breathing Trials (SBTs) or Ventilator Liberation Trials (VLTs) that are intended to encourage diaphragm use and strengthening over time.Therefore, Lungpacer DPT efficacy evaluation must be compared to standard of care in a Control group. Lack of recovery from mechanical ventilation may be due to the inability of a patient to participate in VLTs or weaning attempts, due to extensive diaphragm weakness or sedation, the inability of VLTs to induce sufficient diaphragm strengthening, or co-morbidities that prevent recovery.

Enrollment: 223 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Are 18 years or older, and,
2. Have been mechanically ventilated for ≥96 hours (4 days), and,
3. Have satisfied the Readiness-to-Wean criteria, and,
4. Have failed at least 2 weaning attempts (that were conducted at least 48 hours after initiation of MV, and, that were conducted on different calendar days, and, at least one of which was the protocol-specific Ventilator Liberation Trial).

Exclusion criteria

1. MIP (absolute value) >50 cm H2O;
2. Invasive mechanical ventilation >90 days;
3. Currently on ECMO;
4. Weaning failure due to hypervolemia;
5. Medical history (including imaging) or known anatomy that prevents percutaneous insertion of the Catheter into the intended thoracic vein on the left side.
6. Clinically overt congestive heart failure that is preventing weaning;
7. Currently being treated with neuromuscular blockade;
8. Pre-existing neurological, neuromuscular or muscular disorder that could affect the respiratory muscles;
9. Pre-existing severe chronic pulmonary fibrosis;
10. Pleural effusions occupying greater than one third of the pleural space on either side;
11. BMI >45 kg/m2;
12. Known or suspected phrenic nerve paralysis;
13. Any electrical device (implanted or external) that may be prone to interaction with, or interference from the Lungpacer DPTS including neurological pacing/stimulator devices, cardiac pacemakers and defibrillators;
14. Current hemodynamic instability, sepsis or septic shock;
15. Prior bacteremia reported within the last 48 hours;
16. Anticipating withdrawal of life support and/or shift to palliation as the goal of care;
17. Known or suspected to be pregnant or lactating;
18. Currently being treated in another clinical trial studying an experimental treatment that could affect the study primary outcome.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

223 participants in 2 patient groups

Treatment

Active Comparator group

Description:

Subject receives Lungpacer Catheter for transvenous phrenic nerve stimulation to deliver Diaphragm Pacing Therapy Sessions. DPT sessions are 6 sets of 10, delivered twice daily, for a total of 120 stimulation reps per day, plus standard of care for weaning from mechanical ventilation.

Treatment:

Device: Lungpacer Diaphragm Pacing Therapy

Control

No Intervention group

Description:

Subject does not receive Lungpacer Catheter or DPT. Subject receives only Standard of care for weaning from mechanical ventilation.