Clinical Trials Directory

Trials / Completed

CompletedNCT01700478

Study of the Use of Misoprostol to Decrease Bleeding During a Myomectomy

A Trial Comparing The Use Of Rectal Plus Perivascular Vasopressin With Perivascular Vasopressin Alone To Decrease Bleeding At The Time Of Myomectomy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
45 (actual)
Sponsor
University Hospital of the West Indies · Academic / Other
Sex
Female
Age
25 Years – 40 Years
Healthy volunteers
Accepted

Summary

This study was done to determine if the use of a combination of preoperative rectal misoprostol 400µg used with intraoperative perivascular vasopressin is better than perivascular vasopressin used alone to decrease bleeding at myomectomy.

Detailed description

A myomectomy is a fertility sparing procedure in which fibroids are removed from the uterus. This procedure can be associated with significant blood loss which can result in significant morbidity and mortality. The drug misoprostol which has been been use in the treatment of postpartum hemorrhage was given to subset of patients who were scheduled to undergo elective myomectomy at the University hospital of the West Indies and from the private practice of the participating doctors who were invited to participate in the study. Patients were randomized to receive or not to receive pre-operative rectal misoprostol 400µg, 60 minutes before surgery. Twenty five patients received misoprostol and twenty patients did not.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostol + vasopressin400ug of misoprostol is given per rectum, one hour prior to surgery. Vasopressin is used at the time of surgery.
DRUGVasopressinVasopressin was used in all patients during surgery.

Timeline

Start date
2005-02-01
Primary completion
2005-04-01
Completion
2005-04-01
First posted
2012-10-04
Last updated
2013-02-11

Locations

1 site across 1 country: Jamaica

Source: ClinicalTrials.gov record NCT01700478. Inclusion in this directory is not an endorsement.