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Clinical Trials/NCT00263770
NCT00263770CompletedNot Applicable

A Randomized, Controlled Treatment Trial of Soft Palatal Implants and Positive Airway Pressure in Mild to Moderate Obstructive Sleep Apnea and Snoring

Mayo Clinic1 site in 1 country64 target enrollmentStarted: December 1, 2005Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
64
Locations
1
Primary Endpoint
apnea-hypopnea index

Study Overview

Brief Summary

The purpose of the study is to compare the effectiveness of soft palatal implants with placebo and continuous positive airway pressure treatment in obstructive sleep apnea.

Detailed Description

Obstructive sleep apnea (OSA), frequently associated with disruptive snoring, is a prevalent disorder which is increasingly recognized by health care providers and lay people alike as an important factor in impaired daytime executive function as well as cardiovascular disease risk. Along with an increase in its recognition and diagnosis have come a growing pool of patients with milder disease and the associated challenge of ideal management. Positive airway pressure (PAP) is well established as the mainstay of treatment for OSA since it is effective at reversing daytime neurocognitive sequelae and may be a useful adjunct to therapy in those with cardiovascular disease coexisting with OSA. In patients with mild OSA, however, the response to PAP therapy appears muted, which is related in part to poor adherence to treatment. In response, a number of alternative treatments have evolved. The most recent innovation is soft palatal implants, which, in non-randomized, uncontrolled studies have demonstrated reasonable efficacy in the treatment of snoring and mild to moderate OSA. How the implants compare with standard therapy and their effect on cardiovascular variables are unknown. Because of the ease and rapidity with which this system is implanted, and because treatment effect is independent of patient compliance, there is high potential for widespread use in patients with milder OSA. We therefore are conducting a randomized, placebo-controlled clinical trial to compare the impact of palatal implants with PAP on sleep disordered breathing, daytime symptoms and blood pressure, as well as patient / bed partner acceptance.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age >18 yrs
  • •Tonsil size <50% of airway
  • •No anatomically fixed nasal stenosis
  • •BMI = 32 kg/m2

Exclusion Criteria

  • •The presence of a concomitant untreated primary sleep disorder (restless legs syndrome, narcolepsy, idiopathic hypersomnia)
  • •Severe daytime sleepiness (history of sleep-related motor vehicle or occupational accident)
  • •Moderate to severe pulmonary disease (FEV1 <50% pred)
  • •Neurologic impairment (h/o CVA, TIA, neuromuscular disease, diaphragmatic paralysis)
  • •Significant cardiac disease (LVEF<50%, moderate to severe valvular disease)
  • •Uncontrolled hypertension >180/110
  • •Renal disease (Scr > 2.5)
  • •Allergy to local anesthetics used for implantation procedure.
  • •Pregnant or nursing women

Arms & Interventions

Positive airway pressure (PAP)

Other

which is air delivered by a mask worn over the nose during sleep

Intervention: Positive airway pressure (PAP) (Other)

outpatient surgical procedure

Active Comparator

where small fabric rods are inserted into the soft palate (the fleshy portion of the roof of the mouth) to stiffen the tissues.

Intervention: soft palate implant (Device)

Sham surgery

Sham Comparator

an outpatient surgical procedure identical to #2 except that no rods are inserted into the soft palate.

Intervention: soft palate implant (Device)

Outcomes

Primary Outcomes

apnea-hypopnea index

Time Frame: 90 days

Secondary Outcomes

  • sleepiness(90 days)
  • quality of life(90 days)
  • ambulatory blood pressure(90 days)
  • snoring(90 days)

Investigators

Sponsor Class
Other

Study Sites (1)

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