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
| Type | Name | Description |
|---|---|---|
| DRUG | Terlipressin | Terlipressin 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.) |
| DRUG | normal saline | Patients 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.