Current partner codePEPTIDESDE
NCT07460908·Not applicable·INTERVENTIONAL

Comparison of Terlipressin Versus Octreotide in Patients With Hepatorenal Syndrome

Status

Completed

Phase

Not applicable

Enrollment

60

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

Hepatorenal syndrome is a serious complication of advanced liver disease in which kidney function rapidly worsens and can lead to life-threatening illness. Effective treatment is essential because delayed improvement in kidney function is associated with poor short-term outcomes. This randomized controlled trial will compare two commonly used medicines, terlipressin and octreotide, for the treatment of hepatorenal syndrome in adult patients admitted to Medical Unit III, Lahore General Hospital, Lahore. A total of 60 eligible patients (30 to 70 years of age) will be enrolled using consecutive sampling and randomly allocated in a 1:1 ratio to receive either terlipressin or octreotide according to the study protocol. The main study outcome will be treatment response within 48 hours, assessed by change in serum creatinine. Response will be categorized as complete (serum creatinine less than 1.5 mg/dL at 48 hours), partial (more than 50% reduction from baseline but serum creatinine remains above 1.5 mg/dL), or no response (less than 50% reduction from baseline). It is hypothesized that there is a difference in the clinical response between terlipressin and octreotide in patients with hepatorenal syndrome.

Interventions

Treatment arms and agents.

DRUG

terlipressin

Dose and route: 2 mg intravenous bolus, followed by 1 mg intravenously every 6 hours Treatment duration for primary assessment: 48 hours

DRUG

Octreotide (drug)

Dose and route: 100 micrograms intravenous bolus, prepared as 1 microgram per 1 mL in 0.45% dextrose saline Treatment duration for primary assessment: 48 hours

Timeline

From registration to results.

  1. First posted

    Mar 10, 2026

  2. Study start

    May 1, 2025

  3. Primary completion

    Oct 30, 2025

  4. Study completion

    Oct 30, 2025

  5. Results posted

    Not reported

  6. Registry updated

    Mar 10, 2026

Outcomes

What the study measures.

Primary outcomes

Treatment response based on serum creatinine at 48 hours

Time frame · Baseline and 48 hours after initiation of treatment

Treatment response will be assessed using the change in serum creatinine from baseline to 48 hours after initiation of study drug. Response will be categorized as: Complete response: serum creatinine \< 1.5 mg/dL at 48 hours Partial response: \> 50% decrease in serum creatinine from baseline, but serum creatinine remains \> 1.5 mg/dL at 48 hours No response: \< 50% decrease in serum creatinine from baseline at 48 hours

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
30 Years
Maximum age
70 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Age 30 to 70 years * Either gender * Diagnosed with hepatorenal syndrome Exclusion Criteria: * Hepatocellular carcinoma * Septic shock * Cardiac failure * Respiratory failure * Stroke * Coronary artery disease

Study locations

1 registered sites.

Pakistan. Showing up to 24 locations stored in the fast local snapshot.

Lahore General Hospital, Lahore

Lahore, Punjab Province, Pakistan

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 Vasopressin.

Related PeptideStat pages

Put the record in context.

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