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A Combined Surgical and Medical Approach in Mild Sleep Apnea

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00497120
Enrollment
Unknown
Registered
2007-07-06
Start date
Unknown
Completion date
Unknown
Last updated
2007-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea

Keywords

sleep apnea, snoring, acetazolamide, uvulopalatopharyngoplasty, daytime sleepiness, upper airway

Brief summary

The aim of the study is to investigate wether the adjuvant (postoperative) administration of acetazolamide can improve the surgical results after uvulopalatopharyngoplasty in patients with mild sleep apnea.

Interventions

DRUGacetazolamide
DRUGplacebo
PROCEDUREuvulopalatopharygoplasty

Sponsors

University Hospital, Antwerp
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 5 ≤ Apnea Hypopnea Index (AHI) \< 20 * Socially disturbing snoring: Visual Analogue Scale (VAS)snoring \> 6/10 * Based on clinical examination and polysomnography, patient is regarded eligible for uvulopalatopharyngoplasty (UPPP)

Exclusion criteria

* Previous surgical treatment for sleep-disordered breathing. * Periodic Limb Movement Disorder (PLMD) with arousals and other reasons possibly explaining the Excessive Daytime Sleepiness (EDS) based on Epworth Sleepiness Scale (ESS). * Forced expiratory volume in 1 second (FEV1) \< 80 % pred. * Echocardiography: ejectionfraction \< 35 % or dyastolic dysfunction grade 2 or more.

Design outcomes

Primary

MeasureTime frame
Polysomnographic parameters

Secondary

MeasureTime frame
subjective sleepiness
subjective snoring
satisfaction

Countries

Belgium

Contacts

Primary ContactWilfried De Backer, MD PhD
wilfried.debacker@ua.ac.be+32 3 821 34 47

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026