CTRI/2023/10/058875
Recruiting
未知
se of vasopressin versus phenylephrine to reduce blood loss during laparoscopic myomectomy- a randomised controlled trial. - NI
All india institute of medical sciences Patna0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and Surgical
- Sponsor
- All india institute of medical sciences Patna
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Age between 15\-49 years.
- •2\.BMI between 18\-29\.9\.
- •3\.1\-5 symptomatic intramural myomas
- •4\.Presenting with abnormal uterine bleeding, pelvic pressure or pain, infertility or recurrent miscarriage and are candidates for abdominal myomectomy.
- •5\.Largest uterine fibroid size of \<10 cm
- •6\.not pregnant at the time of presentation (i.e. negative urine pregnancy test or last menstrual period within the last 4 weeks);
- •7\.appropriate medical status for laparoscopic surgery (American Society of Anesthesiologists Physical Status Classification 1 or 2\).
Exclusion Criteria
- •1\.History of previous abdominal or pelvic surgery except Cesarian section.
- •2\.History of pelvic or ovarian endometriosis or abdominal tuberculosis.
- •3\.Patient with subserous or submucosal fibroid or adenomyoma.
- •4\.Patients who are not candidate for laparoscopic myomectomy.
- •5\.any pelvic abnormalities requiring concomitant surgery
- •6\.myoma with a maximal diameter of 10 cm based on pre\-operative ultrasound
- •7\.Allergy to phenylephrine and vasopressin
- •8\.Hypertension, Diabetes Mellitus, Cardiac and pulmonary diseases. (ASA \>2\)
- •9\.Obesity BMI \> 30 kg/m².
- •10\.Anemia Hb \< 10 g/dL.
Outcomes
Primary Outcomes
Not specified
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