HighCycle Study: Effect of Acetazolamide on Plasma Volume During Acute Exposure to High Altitude in Women and Men
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 270
- 试验地点
- 1
- 主要终点
- Plasma volume
研究概览
简要总结
Each year, millions of people living at low altitude (< 1,000 m) travel to high altitude (≥ 2,500 m) for work, tourism, or sports activities. These individuals are exposed to hypobaric hypoxia, which can trigger acute mountain sickness (AMS)-the most common form of altitude-related illness. Therefore, understanding the physiological responses to hypoxia that allow acclimatization, as well as the pathophysiology of acute mountain sickness, is of primary importance.
The hematological response to high-altitude exposure initially includes a reduction in plasma volume (PV), leading to an early increase in hemoglobin concentration within the first 24 hours. In contrast, an increase in hemoglobin mass requires several weeks at high altitude. Recent well-controlled physiological studies conducted in hypobaric chambers have demonstrated that this hypoxia-induced PV contraction results from fluid redistribution from the intravascular to the extravascular compartment, rather than from water loss due to increased diuresis.
Prophylaxis of AMS is primarily based on the administration of 250 mg/day of acetazolamide (ACZ), a carbonic anhydrase inhibitor with a mild diuretic effect. Acetazolamide induces metabolic acidosis, which stimulates ventilation and thereby improves oxygenation. The effect of prophylactic ACZ use during high-altitude exposure on PV in lowlanders remains unknown: it is unclear whether ACZ leads to a greater reduction in PV due to its diuretic effect, or to a smaller hypoxia-induced PV contraction as a result of improved oxygenation induced by increased ventilation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 44 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy, non-smoking men and women, age 18-44 years, without any disease and need of regular medication (including oral contraceptives).
- •BMI >18 kg/m2 and <30 kg/m
- •Born, raised and currently living at altitudes <1000 m.
- •Written informed consent.
- •Premenopausal women with an eumenorrheic cycle.
排除标准
- •Other types of contraceptvies (contraceptives (hormonal intrauterine device, vaginal ring, subcutaneous injections or implants, among others).
- •Pregnancy or nursing
- •Anaemic (haemoglobin concentration <10g/dl).
- •Any altitude trip <4 weks before the study.
- •Allergy to acetazolamide and other sulfonamides.
研究组 & 干预措施
Acetazolamide
Acetazolamide 250 mg/day (capsules @125 mg; 1 in the morning, 1 in the evening), orally. Medication starts 24 hours before ascent to 3600 m until the morning after the second night at 3600 m
干预措施: Acetazolamide (Drug)
Placebo
Placebo (capsules identically looking as acetazolamide capsules; 1 in the morning, 1 in the evening), orally. Medication starts 24 hours before ascent to 3600 m until the morning after the second night at 3600 m.
干预措施: Placebo (Drug)
结局指标
主要结局
Plasma volume
时间窗: Day 1 at 760 m then Day 2 and Day 3 at 3,600 m.
Change in plasma volume assessed by the CO-rebreathing method in acetazolamide versus placebo group
次要结局
- Plasma volume : sex-related difference(Day 1 at 760 m then Day 2 and Day 3 at 3600 m.)
- Plasma volume : AMS-related difference(Day 1 at 760 m then Day 2 and Day 3 at 3600 m.)
- Hormones(Day 2 at 760 m and Day 2 at 3600 m.)
- Arterial blood gases(Day 2 at 760 m and Day 2 at 3600 m.)
