None listed
Conditions
Brief summary
Nocturnal ventilatory support in obesity hypoventilation syndrome study has been completed now
Interventions
Patients randomised to either CPAP or bilevel ventilatory support over a three month period.
Sponsors
Woolcock Institute of Medical Research
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
BMI 30 or above; PaCo2 45mm Hg or above; without major lung or neuromuscular disease to explain awake hypoventilation.
Exclusion criteria
Clinical instability, major psychiatric disorder, patients already using CPAP or bilevel therapy, inability to read or understand the patient information or consent forms.
Outcome results
None listed