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Clinical Trials/CTRI/2023/10/058875
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
All india institute of medical sciences Patna

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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