Feasibility Study to Determine the Effects of Phrenic Nerve Stimulation in Patients With Periodic Breathing

Respicardia

Status and phase

Completed

Phase 1

Conditions

Cheyne-Stokes Respiration

Sleep Disordered Breathing

Sleep Apnea

Treatments

Device: Phrenic stimulation device

Study type

Interventional

Funder types

Industry

Identifiers

NCT00909259

CCI-Feasibility

Details and patient eligibility

About

The purpose of this feasibility study is to determine the effect of stimulating the phrenic nerve to treat periodic breathing (a pattern of breathing characterized by hyperpneas followed by hypopneas or apneas). Clinically, these physiologic events translate into sleep fragmentation, excessive daytime sleepiness, reduced exercise capacity, and possibly ventricular arrhythmias.

Stage 1 of the study is acute in nature, such that subjects will undergo the placement of a stimulation lead, followed by assessment of stimulation of the phrenic nerve using the lead for up to 2 nights of sleep. A sensing lead may also be placed during the initial implant procedure. Observational data will be obtained and stimulation provided using an externalized system connected to the study leads. Following the study, all investigational components will be removed from the patient.

Stage 2 of the study is being conducted at one of the participating sites to determine the initial safety of chronic stimulation of the phrenic nerve in a limited number of patients with sleep disordered breathing. It is anticipated that data obtained in this feasibility study will show that the proposed intervention can modify respiration with a low incidence of adverse effects. The results of this trial are intended to be used to develop a subsequent protocol for a multi-center study of chronic phrenic nerve pacing.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient is 18 years of age or older
Patient has a demonstrated history of periodic breathing (symptoms may include sleep fragmentation, as reported by patient or as witnessed by another person, night arousal after apneic episodes, reduced exercise capacity, and daytime sleepiness)
Patient is expected to be able to tolerate the procedure and remain clinically stable for the duration of the study (e.g. the subject is able to lie down long enough to insert the lead(s) without shortness of breath and the subject is able to tolerate instrumentation during study).
Patient or their legal representative is willing and able to sign an IRB/MEC approved informed consent (and a privacy protection authorization in the United States)

Exclusion criteria

Baseline oxygen saturation less than or equal to 90% on a stable FIO2
Evidence of phrenic nerve palsy
Temperature > 38.0 degrees Celsius
Inability to place catheter (e.g. previously known coagulopathy, distorted anatomy, etc.)
Patient is currently enrolled in another study that may confound the results of this study
Patient for whom informed consent cannot be obtained
Patient who is pregnant or of child bearing potential without a negative pregnancy test within 10 days of the study procedure
Patients implanted with a pacemaker, implantable defibrillator, or cardiac resynchronization device who are unable to tolerate turning off the device for the duration of the system testing procedure (based on medical judgment)
Patients with severe COPD (per GOLD scale)
Patients with a history of myocardial infarction within 6 months prior to the study
Patients with unstable angina
Patients who are intolerant of or allergic to contrast dye
Patients who are contraindicated for <1mg of steroid (on the stimulation lead).