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临床试验/NCT07118462
NCT07118462招募中4 期

HighCycle Study: Effect of Acetazolamide on Plasma Volume During Acute Exposure to High Altitude in Women and Men

Centre d'Expertise sur l'Altitude EXALT1 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2024年7月15日最近更新:
干预措施
相关药物

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

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

Experimental

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 Comparator

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.)

研究者

发起方
Centre d'Expertise sur l'Altitude EXALT
申办方类型
Other
责任方
Sponsor

研究点 (1)

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