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临床试验/NCT02468752
NCT02468752已完成2 期

Mängden kvävgasbubblor i Blodet Efter Dykning Vid Syrgasandning jämfört Med Luftandning

Göteborg University2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2015年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
48
试验地点
2
主要终点
Venous gas emboli

研究概览

简要总结

Primary objective:

  • Assessment of venous gas emboli load post diving when breathing normobaric oxygen compared to air.

Secondary objective:

  • Assessment of fluid markers of central nervous system injury in blood post diving
  • Assessment of fluid markers of inflammation and endothelial dysfunction in blood post diving

Tertiary objective:

  • Assessment of DCS frequency

详细描述

This is a prospective, double blinded, randomized, cross-over study in Sweden. The study was performed in two different sets, each containing standardized dives in a wet hyperbaric chamber. The dives included movement on depth.

In each study set 16-32 professional divers performed no-decompression dives to a depth of 42 metres of seawater (msw). The gas used during the dives was compressed air.

After surfacing the divers breathed either normobaric oxygen or normobaric air on a demand mask. Timing of oxygen/air-breathing differed between study sets. The content of breathing gas was unknown to both divers and examining personnel.

Immediately post dive the divers were assessed using either transthoracic doppler ultrasound (TTD) or transthoracic 2-D ultrasound (TTE) to determine VGE load, time to VGE detection and VGE duration.

Signs of DCS were actively sought.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Professional diver
  • Fit to dive according to Swedish Navy standards

排除标准

  • 未提供

研究组 & 干预措施

Air

Sham Comparator

Normobaric air breathing

干预措施: Air (Other)

Oxygen

Experimental

Normobaric oxygen breathing

干预措施: Oxygen (Drug)

结局指标

主要结局

Venous gas emboli

时间窗: 120 minutes

Kisman-Masurel grading

次要结局

  • Inflammatory activity and endothelial dysfunction(120 minutes/ 48 hours)
  • Decompression sickness(24 hours)
  • Markers of central nervous system injury(120 minutes/ 48 hours)

研究者

发起方
Göteborg University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Nicklas Oscarsson

MD

Göteborg University

研究点 (2)

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