CompletedPhase 2ACTRN12612000113853

Surfactant for Obstructive Sleep Apnea in Patients with Primary Sjogren’s Syndrome: A randomised, placebo controlled study.

Surfactant for OSA in Patients with Primary Sjogren’s Syndrome for improvement of AHI and Sicca Symptoms: A randomised, placebo controlled study.


Sponsor

Adelaide Institute for Sleep Health

Enrollment

14 participants

Start Date

Apr 18, 2011

Study Type

Interventional

Conditions

Summary

Our group has recently found that women with primary Sjogren’s syndrome (an autoimmune disease causing dry eyes and mouth) are considerably more likely to suffer obstructive sleep apnoea (OSA) compared to women without Sjogren’s syndrome. OSA is a common condition in which the upper airway repeatedly closes during sleep and can lead to severe daytime sleepiness, one of the common problems reported by Sjogren’s sufferers. A likely key cause of OSA in Sjogren’s syndrome is reduced and stickier airway secretions that may predispose to airway obstruction and disturbed sleep at night. Recent research in OSA patients without Sjogren’s syndrome has shown that lubricating the upper airway with a substance called surfactant improves OSA. Surfactants are naturally produced in the lung and work by decreasing the “stickiness” (surface tension) of fluids. Therefore, at least in OSA patients without Sjogren’s syndrome, surfactants applied to the upper airway appear to help the airway to stay open and reopen more easily if it becomes closed. Women with Sjogren’s syndrome are likely to similarly benefit from this form of treatment. The aim of this study is to determine whether the topical application of surfactant in women with primary Sjogren’s Syndrome who have obstructive sleep apnoea as well, will reduce the severity of their OSA and salivary stickiness and will improve their symptoms of overnight dryness and general morning well-being or not.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This randomised, placebo-controlled study tests whether surfactant therapy can help treat obstructive sleep apnea in patients who also have Primary Sjogren's Syndrome (an autoimmune condition that causes dryness). Adults aged 18 and over with both conditions may be eligible.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Surfactant (abbott's Survanta) 4.0mls topically into upper airways(half the dose via oropharynx and half via nasopharynx). The dose was given at baseline prior to sleep onset and repeated 3.5 hours af

Surfactant (abbott's Survanta) 4.0mls topically into upper airways(half the dose via oropharynx and half via nasopharynx). The dose was given at baseline prior to sleep onset and repeated 3.5 hours after sleep onset. On the consecutive night surfactant will be crossed over by 4.0 mls of 0.9 % normal saline via same route and with same frequency.


Locations(1)

Australia

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12612000113853