Current partner codePEPTIDESDE
NCT03130127·Not applicable·INTERVENTIONAL

Continuous Versus Bolus Infusion of Terlipressin for Portal Hypertension Related Bleeding in Liver Cirrhosis

Status

Unknown

Phase

Not applicable

Enrollment

40

Locations

0

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

Terlipressin is the mainstay drug for the treatment of acute variceal bleeding in liver cirrhosis. According to the drug instructions, intravenous bolus infusion is the standard approach of terlipressin. It remains unclear about whether or not continuous infusion of terlipressin should be considered.

Full detailed description

Although intravenous bolus infusion of terlipressin is the standard approach, continuous infusion of terlipressin is preferred in clinical practice. The present study is a pilot non-randomized controlled trial to explore the feasibility and safety of continuous infusion of terlipressin for the treatment of acute variceal bleeding in liver cirrhosis.

Interventions

Treatment arms and agents.

DRUG

Terlipressin

According to the current practice guidelines and consensus, terlipressin is the standard treatment option for acute variceal bleeding in liver cirrhosis.

Timeline

From registration to results.

  1. First posted

    Apr 26, 2017

  2. Study start

    Jul 1, 2024

  3. Primary completion

    Dec 1, 2025

  4. Study completion

    Dec 1, 2025

  5. Results posted

    Not reported

  6. Registry updated

    Feb 23, 2024

Outcomes

What the study measures.

Primary outcomes

5 day treatment failure

Time frame · 5 days (120 hours)

Death, fresh hematemesis, hypovolaemic shock, or 3 g drop in Hb (9% drop of Ht) within any 24 h period if no transfusion is administered.

Secondary outcomes

Six-week mortality

Time frame · 6 weeks

Death with 6 weeks after treatment

Eligibility

Who can take part.

Minimum age
Not reported
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: 1. A diagnosis of liver cirrhosis; 2. Child-Pugh B or C; 3. Acute gastroesophageal variceal bleeding; 4. Written informed consents. - Exclusion Criteria: 1. No liver cirrhosis; 2. Child-Pugh class A; 3. Acute upper gastrointestinal bleeding unrelated to varices; 4. Use of somatostatin or octreotide. -

Study locations

0 registered sites.

No country data reported. Showing up to 24 locations stored in the fast local snapshot.

No study locations reported.

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Terlipressin.

Related PeptideStat pages

Put the record in context.

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