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NCT06085976

Efficacy and Safety of Octreotide in Laparoscopic Hepatectomy Surgery: Effect on Blood Loss, Need for Vasoactive Drugs, Transfusion Requirements.

Status unknown Phase 2 Last updated 17 October 2023
What this trial tests

Phase 2 trial testing Octreotide in Hepatic Carcinoma in 62 participants. Status unknown.

Timeline
14 August 2023
Primary endpoint
14 August 2025
30 November 2025

Quick facts

Lead sponsorClinica Universidad de Navarra, Universidad de Navarra
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment62
Start date14 August 2023
Primary completion14 August 2025
Estimated completion30 November 2025
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Clinica Universidad de Navarra, Universidad de Navarra

Who can join

Adults 18 to 80, any sex, with Hepatic Carcinoma or Hepatic Metastasis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this double-blind clinical trial is to compare the efficacy of octreotide versus placebo in laparoscopic hepatectomy surgery in patients diagnosed with resectable hepatocarcinoma or liver metastases. The main questions it aims to answer are: * Decrease in intraoperative bleeding measured in ml of blood lost. * Decrease in the need for blood transfusion and use of intraoperative vasoactive drugs. Participants will receive octreotide or placebo after signing the informed consent form.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Octreotide

Trials testing the same drug.

Other recruiting trials for Hepatic Carcinoma

Currently open trials in the same condition.

Other Clinica Universidad de Navarra, Universidad de Navarra trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06085976.

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