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The Effect of Milrinone Combined with Terlipressin on Bleeding and Renal Function during Liver Partial Resection: A Prospective Randomized Controlled Trial

The Effect of Milrinone Combined with Terlipressin on Bleeding and Renal Function during Liver Partial Resection: A Prospective Randomized Controlled Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091761
Enrollment
Unknown
Registered
2024-11-03
Start date
2024-11-03
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Liver cancer, hepatic hemangioma, cholangiocarcinoma and others

Interventions

Milrinone and Teripressin group:After implantation of a double-lumen central venous catheter, Milrinone (12.5ug/kg,10min, i.e. 0.3ml/kg/h,10min) combined with terlipressin (1mg,10min, i.e. 120ml/h,10m
Saline solution group:After the two-cavity central venous catheter was inserted, normal saline (0.3ml/kg/h,10min) combined with normal saline (120ml/h,10min) was pumped, and then normal saline (0.12ml

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) American Society of Anesthesiologists (ASA) Level I-III (2)Age >=18 years old (3) Body mass index (weight divided by height squared) 18~30kg/? (4) Selective liver resection under general anesthesia (hepatectomy refers to the removal of local lesions of the liver due to primary or secondary malignant tumors or benign tumors; the surgical method is open or laparoscopic) (5) Those who can understand and sign the informed consent form

Exclusion criteria

Exclusion criteria: (1) Patients with portal hypertension before surgery (ascites, splenomegaly, thrombocytopenia with platelets 180/100 mmHg after sedation) (11) Currently participating in another interventional study that may affect the primary outcome

Design outcomes

Primary

MeasureTime frame
Intraoperative blood loss;Incidence of postoperative acute kidney injury;

Secondary

MeasureTime frame
Blood transfusion volume;leukocyte;C-reactive protein;platelet;albumin;Hypersensitive troponin;Brain natriuretic peptide;Serum creatinine;Cystatin C;Mean arterial pressure;Heart rate;Central venous pressure;Duration of hypotension;Vasoactive drug use;Minimum central venous pressure;Lactic acid maximum;Infusion volume;Urine volume;Drug-related adverse events;Time of first feeding;First exhaust time;Time of first defecation;Length of stay;Postoperative complication;

Countries

China

Contacts

Public ContactYueying Zhang

The Affiliated Hospital of Xuzhou Medical University

zyy0218@126.com+86 180 5226 8602

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026