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临床试验/NCT00715741
NCT00715741已完成2 期

Does High Intraoperative Inspired Oxygen Reduce Postoperative Arterial Oxygen Saturation?

University of Utah1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2008年6月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
100
试验地点
1
主要终点
Oxygen Requirement to Maintain SpO2>90%

研究概览

简要总结

The purpose of this study is to determine whether breathing high levels of oxygen during surgery affects oxygen levels after surgery. The second purpose of this study is to determine whether giving positive end expiratory pressure PEEP and high oxygen together affects patients oxygen levels after surgery.

详细描述

This is a randomized, controlled, blinded trial in patients undergoing non-abdominal surgery of the effect of intraoperative increased inspired oxygen used (FiO2>0.9 vs. FiO2 = 0.3) on non-invasive oxygen saturation (pulse oximetry, SpO2) and amount of required supplemental oxygen in the post-anesthesia care unit (PACU); arterial oxygen partial pressure (PaO2) after 45 minutes in the PACU; room air SpO2 24 hours after surgery, and amount of supplemental oxygen required 24 hours after surgery. The purpose of the study is to determine whether absorption atelectasis induced by use of inspired oxygen concentrations in excess of 90% leads to a higher risk of hypoxemia, as evidenced by room air oxygen values and the need for supplemental oxygen. The objective of this study is to determine whether high inspired oxygen (>0.8), which has been demonstrated to reduce the risk of surgical site infection in patients undergoing colon surgery and other major surgical procedures has side effects that limit its use to prevent infection in lower risk operations.

There are four groups of intraoperative ventilation management in this study. Fi02 0.3 plus PEEP, Fi02 0.3 without PEEP, Fi02 greater than 0.9 plus PEEP 3 to 5 cm of water, Fi02 greater than 0.9 without PEEP.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients aged 18-70 years undergoing surgery under general endotracheal anesthesia at the University of Utah Hospital Operating Room and the Huntsman Cancer Hospital Operating room who will be admitted to the hospital for at least 24 hours after surgery

排除标准

  • •Major (open) abdominal surgery
  • •Major spine surgery
  • •Craniotomy surgery
  • •Surgeries where electrocautery or laser devices may be used near the airway (eg tracheostomy, oral surgery) because of the risk of fire with high inspired oxygen in these cases
  • •Procedures planned for monitored anesthesia care (MAC) or regional without general anesthesia
  • •Planned airway management with a laryngeal mask airway rather than an endotracheal tube
  • •Procedures planned in the prone position because this increases atelectasis
  • •Planned postoperative intubation
  • •Planned postoperative care in the intensive care unit
  • •Recent (within 3 weeks) chemotherapy because of the increased risk of pulmonary oxygen toxicity
  • •History of bleomycin administration because of the increased risk of pulmonary oxygen toxicity
  • •Diagnosed Obstructive Sleep Apnea with home continuous pulmonary airway pressure (CPAP) use
  • •Home oxygen use
  • •Preoperative room air (RA) SpO2 <90%
  • •History of spontaneous pneumothorax
  • •Emergency surgery
  • •Pregnancy. Women of child-bearing age are routinely screened for pregnancy urine human chorionic gonadotropin, (HCG) on the morning of surgery. Patients with a positive result will be excluded from the study (and most likely will have their elective surgery cancelled).
  • •Patient refusal

研究组 & 干预措施

1

Active Comparator

Group 1 will receive 30% oxygen plus PEEP + 3 to 5 cm Water duration of anesthesia and surgery

干预措施: FiO2 (fraction of inspired oxygen) 0.3 plus PEEP (positive end expiratory pressure) 3 -5 cm water (Other)

2

Active Comparator

Group 2 will receive 30% oxygen without PEEP for the duration of anesthesia and surgery

干预措施: FiO2 0.3 without PEEP (Other)

3

Active Comparator

Group 3 will receive > 90% oxygen plus PEEP + 3 to 5 cm of water for the duration of anesthesia and surgery

干预措施: FiO2 >0.9 with 3-5 cm water PEEP (Other)

4

Active Comparator

Group 4 will receive > 90% oxygen and no PEEP for the duration of anesthesia and surgery

干预措施: FiO2 >0.9 without PEEP (Other)

结局指标

主要结局

Oxygen Requirement to Maintain SpO2>90%

时间窗: 45 min after emergence (tracheal extubation)

Arterial oxygen saturation by pulse oximetry (SpO2) is measured while subject is lying quietly in the post anesthesia care unit (PACU) and breathing room air (RA). Oxygen is added 0.5 liters per min (LPM) at a time to maintain SpO2 \>90%.

Oxygen Requirement

时间窗: 24 hours after tracheal extubation

amount of oxygen (LPM) required to maintain SpO2 \>90%

次要结局

  • Arterial Oxygen Saturation by Pulse Oximetry "(SpO2)"(45 min after tracheal extubation)
  • SpO2 Postoperatively(24 hours after tracheal extubation)

研究者

申办方类型
Other

研究点 (1)

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