A clinical trial of the effect of remimazolam on postoperative ECG in gynecologic laparotomy
- Conditions
- Patients scheduled for gynecologic laparotomy
- Registration Number
- JPRN-jRCT1051220068
- Lead Sponsor
- Hori Kotaro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 120
1) Patients scheduled for genecologic laparatomy
under general anesthesia
2) Patients aged 20 or older
3) Patients classified as ASA-PS 1 or 2 (American Society of Anesthesiologists-Physical Status)
4) Patients who fully understand the study after sufficient explanations and provide the written volun
tary consent
1) Patients who have contraindication or allergy to sevoflurane or remimazolam
2) Patients who have abnormal QT interval in preoperative ECG
3) Patients who do not have sinus rhythm in preoperative ECG
4) Patients who take antipsychotics, antiarrhythmics, or beta-blockers
5) Patients who have hypokalemia (< 3.5 mEq/L) or hyperkalemia (> 5.5 mEq/L) in preoperative labor
atory data
6) Patients whose BMI are 35 or greater
7) Patient who are considered ineligible for enrolling the study by a principal- or co-investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method