Clinical Trials Directory

Trials / Completed

CompletedNCT03572088

Terlipressin Infusion During Whipple Procedure: Effect on Blood Loss and Transfusion Needs

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Assiut University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The present study aims to look at the effect of terlipressin infusion on blood loss and blood transfusion needs during Whipple procedure

Conditions

Interventions

TypeNameDescription
DRUGTerlipressinTerlipressin is a synthetic vasopressin analogue with relative specificity for the splanchnic circulation(Terlipressin was started at the beginning of surgery as an initial bolus dose of 1 mg over 30 mints(1 mg/50 ml normal saline at a rate of 100 ml/h) followed by a continuous infusion of 2 μg/kg/h(1 mg/50 ml at a rate equal to wt/10 ml per hour) and weaned in the postoperative period over 4 hours.)
DRUGnormal salinePatients received 50 ml normal saline at a rate of 100 ml/h followed by a continuous infusion of 50 ml at a rate equal to wt/10 ml per hour and weaned in the postoperative period over 4 hours.

Timeline

Start date
2016-05-01
Primary completion
2017-07-01
Completion
2017-07-01
First posted
2018-06-28
Last updated
2023-05-22

Source: ClinicalTrials.gov record NCT03572088. Inclusion in this directory is not an endorsement.