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Trial · NCT06687265

Effects of Metformin on Hepatic Venous Pressure Gradient in Patients With Cirrhosis and Portal Hypertension

NCT06687265, Phase 2, Recruiting, Assistance Publique - Hôpitaux de Paris

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effects of Metformin on Hepatic Venous Pressure Gradient in Patients With Cirrhosis and Portal Hypertension. Trials, record NCT06687265. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06687265

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Effects of Metformin on Hepatic Venous Pressure Gradient in Patients With Cirrhosis and Portal Hypertension
NCT number
NCT06687265
Status
Recruiting
Phases
Phase 2
Enrollment
76 participants, estimated
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Conditions
Cirrhosis, Portal Hypertension Related to Cirrhosis
Interventions
Metformin, Placebo
First posted
2024-11-13
Last updated
2025-04-13

Source ClinicalTrials.gov

Registered outcomes19

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primaryeffect of metformin versus placebo during 28 days on HVPG, in patients with cirrhosis and a HVPG ≥ 12 mm Hg already treated with carvedilol.after 28 days of treatmentHVPG measures before and after metformin or placebo treatment
Secondarythe rate of patients with a clinically significant improvement in HVPGafter 28 days of treatmentChange in arterial pressure after treatment : HVPG \> or = 12 mm Hg, or at least a 10% reduction from baseline,
SecondaryChange in cirrhosis severity MELD scoreafter 28 days of treatmentMELD (Model for End-Stage Liver Disease) score classification (6-40 with high score is worse outcome)
SecondaryChange in cirrhosis severity Child-Pugh scoreafter 28 days of treatmentChild-Pugh classification or Child-Turcotte-Pugh classification (5-15 with high score is worse outcome)
Secondarychange in systemic haemodynamicsafter 28 days of treatmentThe size (diameter) of a blood vessel.
Secondarythe tolerability of metformin in patients with cirrhosis and a HVPG ≥ 12 mm Hgafter 28 days of treatmenttreatment compliance
SecondaryMaximum metformin plasma levelafter 28 days of treatmentplasma level (at 2h30 of last dose)
SecondaryRelative changes in HVPGday 28HVPG measure
SecondaryChange in arterial pressureafter 28 days of treatmentHVGP
Secondarythe safety of metformin in patients with cirrhosis and a HVPG ≥ 12 mm Hg30 days after the beginning of treatmentcomplication and adverse event evaluate by CTCAE guideline during treatment

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
34165199BACKGROUND

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06687265

GET https://conductscience.org/api/trials/v1/NCT06687265/registered