跳至主要内容
临床试验/NCT06216977
NCT06216977撤回不适用

CODA-POP Surgery: Clears On the Day of Anesthesia Permissible up to One-Hour Prior to Surgery - A Prospective Randomized and Blind Trial

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年1月20日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
入组人数
150
试验地点
2
主要终点
Residual Gastric Volume in mL/kg

研究概览

简要总结

The purpose of this study is to assess whether residual gastric volumes in patients who receive clear liquids one hour prior to time of procedure is non-inferior compared to patients who are NPO past midnight, to compare efficiency and flexibility of operating room scheduling between two fasting conditions, to assess patient satisfaction and post-operative nausea, vomiting, pain, hunger and thirst.

and to assess wound healing and post-operative complication rates.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Care Provider)

入排标准

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

入选标准

  • Undergoing laparoscopic cholecystectomy during the day or night of a weekday (including those consented on a Friday who get postponed to a weekend surgery start time).
  • Modified rapid sequence intubation (mRSI)

排除标准

  • History of reflux disease
  • History of hiatal hernia
  • History of esophageal disease
  • History of gastroparesis
  • Known history of difficult airway or planned fiberoptic intubation
  • HbA1c greater than 12
  • Pregnant women
  • Procedures conducted on weekends and holidays
  • Emergency or non-elective procedures

结局指标

主要结局

Residual Gastric Volume in mL/kg

时间窗: At time of intubation (about 1 hour after fluid intake)

次要结局

  • Number of participants with observed emesis(During perioperative period which includes preoperative, intraoperative and post operative time (about 4 hours))
  • Number of participants with production of oropharyngeal secretions(During the perioperative period which includes preoperative, intraoperative and post operative time (about 4 hours))
  • Number of participants with wound dehiscence(postoperative follow up appointment (about 1 month after surgery))
  • Number of participants with subjective post-operative nausea(within 24 hours of surgery)
  • Overall patient satisfaction as assessed by the Press-Ganey Questionnaire(within 48-96 hours of surgery)
  • Number of participants with intraoperative complications(From start of surgery to end of surgery)
  • Number of participants with subjective pre-operative nausea(at baseline)
  • Amount of post-operative pain medications needed(at first clinic appointment (about 1 month after surgery))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

yafen liang

Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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