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Clinical Trials/JPRN-UMIN000036240
JPRN-UMIN000036240
Completed
未知

Monitoring of stroke volume variation and fluid responsiveness in laparotomy and pneumoperitoneum surgery - Fluid responsiveness in laparotomy and pneumoperitoneum surgery

Shonan Kamakura General Hospital Department of Anesthesia0 sites120 target enrollmentMarch 18, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Gastrointestinal surgery
Sponsor
Shonan Kamakura General Hospital Department of Anesthesia
Enrollment
120
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 18, 2019
End Date
April 1, 2020
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Shonan Kamakura General Hospital Department of Anesthesia

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Patients with a history of myocardial infarction within 30 days prior to surgery 2\) Patients with a history of percutaneous coronary intervention or coronary artery bypass surgery 3\) Patients with unstable angina 4\) Patients with decreased left ventricular function (LVEF\<\=50%) 5\) Patients with a history of cerebrovascular disorder (excluding asymptomatic lacunar infarction) 6\) Patients with a history of hospitalization due to heart failure within 30 days before surgery 7\) Patients with severe liver disease (AST (GOT) or ALT (GPT)\>\=100 U) 8\) Patients with severe kidney disease (BUN\>25 mg / dL or serum creatinine\>\=2\.0 mg / dL) 9\) Patients with sepsis 10\) Borben contraindicated patients 11\) Women who may be pregnant or may become pregnant 12\) A lactating woman 13\) Patients with arrhythmia 14\) In addition, patients whose research managers judged inappropriate based on medical evidence as research subjects

Outcomes

Primary Outcomes

Not specified

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