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Clinical Trials/NCT04387058
NCT04387058UnknownNot Applicable

Incidence of Diabetes and Metabolic Disorders After TIPS in Cirrhotic Patients

University Hospital, Toulouse2 sites in 1 country111 target enrollmentStarted: June 16, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
111
Locations
2
Primary Endpoint
the cumulative incidence

Study Overview

Brief Summary

Decompensated cirrhosis is associated with sarcopenia. TIPS is an efficient treatment of portal hypertension. Based on our retrospective data, TIPS induces in 30% of cirrhotic patients metabolic disorders associated with diabetes or pre-diabetes. The main objective is to measure the cumulative incidence of diabetes and pre-diabetes 6 months after TIPS insertion.

Detailed Description

Based on our retrospective data, we expect that one-third of cirrhotic patients develop glucose dysregulation after TIPS. A better knowledge of the metabolic disorders related to the TIPS could allow to prevent the deleterious effects of the TIPS on the disease (decrease of the insulin-sensitivity, fat gain ...), by simple interventions on diet or physical activity. We will assess the incidence of diabetes and pre-diabetes, and the influence of TIPS on nutritional status and sarcopenia. Patients will be follow-up 6 months after TIPS. We will explore the hormonal mechanisms that explain these changes.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • patient cirrhosis and portal hypertension justifying a treatment with TIPS
  • written consent.

Exclusion Criteria

  • contraindication for TIPS
  • indications of TIPS in emergency or as part of the preparation for a surgical procedure,
  • hepatocellular carcinoma outside Milan criteria or cancer at a palliative stage,
  • a contra-indication to the realization of an OGTT,
  • a hyperglycemic treatment (corticosteroids, somatostatin, etc.),
  • hemoglobin <7 g / dl,
  • patients who have had a liver transplant,
  • those for whom the follow-up is considered impossible or the vital prognosis is engaged in the short term,
  • pregnant or lactating women,
  • those unable to receive enlightened information,
  • those participating in interventional research
  • and finally the persons placed under safeguard of justice, tutelage or curatorship.

Outcomes

Primary Outcomes

the cumulative incidence

Time Frame: 6 months

The primary outcome is the cumulative incidence (%) of diabetes and pre-diabetes observed 6 months after TIPS insertion (M6). Diabetes and pre-diabetes will be defined according to World Health Organization (WHO) criteria, based on fasting blood glucose level or 2h after an oral glucose test

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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