ClinicalTrials.Veeva

Menu
The trial is taking place at:
E

Epic Medical Research | Red Oak, TX

Veeva-enabled site

Treating Obstructive Sleep Apnea Using Targeted Hypoglossal Neurostimulation (OSPREY)

LivaNova logo

LivaNova

Status

Active, not recruiting

Conditions

Hypopnea, Sleep
Apnea, Obstructive Sleep
Apnea
Apnea+Hypopnea
Apnea, Obstructive
OSA
Obstructive Sleep Apnea

Treatments

Device: Hypoglossal Nerve Stimulation

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

Multi-center, open-label, prospective, randomized clinical trial of the aura6000(R) System for the reduction of apnea and hypopneas in adult patients with moderate to severe obstructive sleep apnea who have failed or are unwilling to use positive airway pressure treatment.

Full description

All qualifying subjects will be implanted. Subjects will be randomized 2:1 in favor of Stimulation therapy (Active Group). Randomization will occur following implant and prior to the Month 1 visit.

The Active group will start Stimulation therapy at Month 1. The Control group may continue with their current sleep apnea treatment until Month 7, and will receive Stimulation therapy beginning at Month 7 +1Day. (All subjects are excluded from use of PAP or surgical treatments after enrollment through Month 13)

Safety and efficacy will be evaluated at Month 7, and again at Month 13.

Enrollment

150 estimated patients

Sex

All

Ages

22+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Abbreviated: Additional criteria may apply:

Inclusion Criteria:

  • Diagnosis of moderate to severe OSA
  • Declines to use or does not tolerate PAP therapy

Exclusion Criteria:

  • Respiratory, cardiac, renal disease or other co-morbid conditions
  • BMI > 35 kg/m2
  • Specific PSG criteria outlined in the protocol

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

150 participants in 2 patient groups

Active
Active Comparator group
Description:
HGN therapy activation at Month 1 - compared at Month 7 to Control group, continued stimulation through Month 13
Treatment:
Device: Hypoglossal Nerve Stimulation
Control
Other group
Description:
HGN therapy NOT activated at Month 1 - compared at Month 7 to Active group, stimulation will start at Month 7 + 1 Day and continue through Month 13
Treatment:
Device: Hypoglossal Nerve Stimulation

Trial contacts and locations

20

Loading...

Central trial contact

Amy Keith; Nadine Juran, BSN, RN

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems