Effect of Acetazolamide on Central Sleep Apnea Related to Opium Consumption
Central Sleep Apnea, Secondary
About this trial
This is an interventional treatment trial for Central Sleep Apnea, Secondary focused on measuring Acetazolamide, Central Sleep Apnea, Opium Abuse
Eligibility Criteria
Inclusion Criteria:
- Opium or opioid use for at least two months in a daily manner
- Presence of five or more central sleep apnea per hour in a full-night recorded PSG
Exclusion Criteria:
- Congestive heart failure
- living in high altitude
- Chronic Obstructive Pulmonary Disease (COPD)
- Carbon dioxide partial pressure (pCO2) elevation due to other respiratory diseases
- Body Mass Index (BMI) > 32
- Obesity Hypoventilation Syndrome
- Severe renal or liver disorders
- Using Benzodiazepine
- Using Theophylline
Sites / Locations
- Masih Daneshvari Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
#1 (Acetazolamide-placebo)
#2 (Placebo-acetazolamide)
The arm #1 consists of 6 eligible patients who receive Acetazolamide 250mg once daily an hour before sleep for first six nights and after two weeks washout they receive placebo for six nights in the same order. After each six-day period they undergo polysomnography.
The arm #2 consists of 6 eligible patients who receive placebo once daily an hour before sleep for first six nights and after two weeks washout they receive acetazolamide 250mg for six nights in the same order. After each six-day period they undergo polysomnography.