Skip to content

Effects of Terlipressin on Blood Loss and Transfusion Requirements During Major Liver Resection.

Effects of Terlipressin on Blood Loss and Transfusion Requirements During Major Liver Resection.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02588716
Enrollment
84
Registered
2015-10-28
Start date
2015-09-30
Completion date
2016-12-31
Last updated
2017-12-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatectomy, Surgical Blood Loss, Terlipressin

Keywords

Hepatectomy, Surgical Blood Loss, terlipressin

Brief summary

To evaluate the effects of Terlipressin infusion on blood loss & transfusion requirements in cirrhotic patients undergoing major liver resections.

Interventions

DRUGTerlipressin

Terlipressin will be given as an intravenous injection of 2μg/kg/h to be continued throughout the surgery and weaned off over four hours postoperatively.

DRUGnormal saline

Same volumes of normal saline infusion, throughout the operation then gradually withdrawn over 4 hours.

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients older than 18 years of age, American Society of Anesthesiology (ASA) classification class I and II and assigned for elective resection of 2 or more liver segments portal hypertension

Exclusion criteria

* Patients with Child-Turcotte-Pugh grade B or C, clinically significant portal hypertension (splenomegaly, thrombocytopenia with platelets \< 1011/L, esophageal varices grade 2 or more), Preoperative renal failure (GFR \< 50ml/min), heart failure, Bradyarrhythmia (heart rate \< 60/min), history of hemorrhagic stroke, Uncontrolled arterial hypertension (Blood pressure \>160/100mmHg), and Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
blood lossintraoperative periodblood loss in ml

Secondary

MeasureTime frameDescription
blood units transfusedintraoperative periodnumber of packed RBCs units transfused
lactate levelat start and end of resectionlactate level in blood gas sample in mmol/L

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026