Status:
COMPLETED
Comparison of Concentration of Vasopressin During Robot-assisted Laparoscopic Myomectomy
Lead Sponsor:
Seoul National University Hospital
Collaborating Sponsors:
CHA University
Conditions:
Uterine Leiomyoma
Eligibility:
FEMALE
19-60 years
Phase:
NA
Brief Summary
The purpose of this study is to compare the effect of the concentration of vasopressin, which is used as a method for reducing blood loss in robot-assisted laparoscopic myomectomy.
Detailed Description
This study is to compare the effect of the concentration of vasopressin, which is used as a method for reducing blood loss in robot-assisted laparoscopic myomectomy. We would like to evaluate the feas...
Eligibility Criteria
Inclusion
- Informed consent
- Age: 19-60 year-old women
- Plan of myomectomy for uterine leiomyomas
- Leiomyoma Subclassification System 2-7 (robot-assisted laparoscopic myomectomy is possible)
- American Society of Anesthesiologists Physical Status classification 1 or 2
- A person who understands the contents of the clinical trial, is cooperative with the trial, and is judged to be able to participate until the end of the study
Exclusion
- Pregnancy or breastfeeding
- A single diameter of uterine leiomyoma is greater than 12 cm or more or multiple leiomyomas with more than five
- Suspicious disease of uterine malignancy
- Patient with has a history of pelvic surgery (cesarean section, myomectomy, etc.) and is expected to have severe pelvic adhesion
- A person who is hypersensitive or contraindicated to vasopressin
- A person who is hypersensitive or contraindicated to tranexamic acid
- Considered as inappropriate by the researcher's judgment
Key Trial Info
Start Date :
May 10 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 31 2022
Estimated Enrollment :
39 Patients enrolled
Trial Details
Trial ID
NCT04874246
Start Date
May 10 2021
End Date
December 31 2022
Last Update
June 26 2023
Active Locations (1)
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1
Seoul National University Hospital
Seoul, South Korea, 03080