Transcranial Doppler Ultrasound and Minimal Hepatic Encephalopathy

Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Completed
CT.gov ID
NCT04077125
Collaborator
(none)
100
1
13.4
7.5

Study Details

Study Description

Brief Summary

Minimal hepatic encephalopathy (MHE) is a subclinical complication of liver cirrhosis with a relevant social impact. Thus, there is urgent need to implement easy to use diagnostic tools for the early identification of affected patients.

This study was aimed to investigate cerebral blood flow, systemic hemodynamics as well as endothelial function of cirrhotic patients with MHE, and to verify their change after treatment with rifaximin.

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Observational
Actual Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Minimal Hepatic Encephalopathy is Associated With Increased Cerebral Vascular Resistance. a Transcranial Doppler Ultrasound Study
Actual Study Start Date :
Jan 18, 2018
Actual Primary Completion Date :
Dec 31, 2018
Actual Study Completion Date :
Mar 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Cirrhosis no MHE

Patients with liver cirrhosis without signs of minimal hepatic encephalopathy

Cirrhosis MHE

Patients with liver cirrhosis with minimal hepatic encephalopathy

Drug: Rifaximin
to investigate changes in cerebral, splanchnic hemodynamics and endothelial function in cirrhotic patients with MHE after 15 days of rifaximin therapy (1200 mg/d)

Controls

Healhty subjects

Outcome Measures

Primary Outcome Measures

  1. Quantification of middle cerebral artery resistive index [baseline]

    Quantification of middle cerebral artery resistive index by Doppler ultrasound in patients with liver cirrhosis with or without MHE

  2. Quantification of middle cerebral artery pulsatility index [baseline]

    Quantification of middle cerebral artery pulsatility index by Doppler ultrasound in patients with liver cirrhosis with or without MHE

  3. Quantification of posterior cerebral artery resistive index [baseline]

    Quantification of posterior cerebral artery resistive index by Doppler ultrasound in patients with liver cirrhosis with or without MHE

  4. Quantification of posterior cerebral artery pulsatility index [baseline]

    Quantification of posterior cerebral artery pulsatility index by Doppler ultrasound in patients with liver cirrhosis with or without MHE

  5. Change in middle cerebral artery resistive index after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Variation of middle cerebral artery resistive index measured by Doppler ultrasound after treatment with rifaximin 1200 mg/d for 15 days in patients with liver cirrhosis and MHE

  6. Change in middle cerebral artery pulsatility index after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Variation of middle cerebral artery pulsatility index measured by Doppler ultrasound after treatment with rifaximin 1200 mg/d for 15 days in patients with liver cirrhosis and MHE

  7. Change in posterior cerebral artery resistive index after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Variation of posterior cerebral artery resistive index measured by Doppler ultrasound after treatment with rifaximin 1200 mg/d for 15 days in patients with liver cirrhosis and MHE

  8. Change in posterior cerebral artery pulsatility index after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Variation of posterior cerebral artery pulsatility index measured by Doppler ultrasound after treatment with rifaximin 1200 mg/d for 15 days in patients with liver cirrhosis and MHE

Secondary Outcome Measures

  1. Comparison of renal artery resistive index of cirrhotic patients with MHE compared to those without [baseline]

    Comparison of renal artery resistive index measured by Doppler ultrasound of cirrhotic patients with MHE and those without

  2. Comparison of splenic artery resistive index of cirrhotic patients with MHE compared to those without [baseline]

    Comparison of splenic artery resistive index measured by Doppler ultrasound of cirrhotic patients with MHE and those without

  3. Comparison of flow mediated dilation of cirrhotic patients with MHE compared to those without [baseline]

    Comparison of endothelial function (flow mediated dilation measured by Doppler ultrasound) of cirrhotic patients with MHE and those without

  4. Change in renal artery resistive index after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Change in renal artery resistive index measured by Doppler ultrasound in patients with liver cirrhosis and MHE after treatment with rifaximin 1200 mg/d for 15 days

  5. Change in splenic artery resistive index after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Change in splenic artery resistive index measured by Doppler ultrasound in patients with liver cirrhosis and MHE after treatment with rifaximin 1200 mg/d for 15 days

  6. Change in flow mediated dilation after treatment with rifaximin [at the end of rifaximin treatment (15 days)]

    Change in endothelial function (flow mediated dilation measured by Doppler ultrasound) in patients with liver cirrhosis and MHE after treatment with rifaximin 1200 mg/d for 15 days

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • diagnosis of liver cirrhosis on the basis of clinical, laboratory and ultrasound findings
Exclusion Criteria:
  • active alcohol abuse (excessive alcohol intake stopped more than 6 months before the enrollment);

  • chronic pulmonary diseases; ongoing infections; cerebrovascular diseases; primary or secondary cerebral neoplasm; primary liver neoplasm; heart function failure; chronic kidney disease; peripheral vascular disease; treatment with rifaximin or systemic antibiotics in the previous 15 days;

  • smoking habit;

  • grade 1 or overt hepatic encephalopathy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondazione Policlinico Agostino Gemelli IRCCS Roma Italy 00168

Sponsors and Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Francesca Ponziani, Principal Investigator, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
ClinicalTrials.gov Identifier:
NCT04077125
Other Study ID Numbers:
  • 1712
First Posted:
Sep 4, 2019
Last Update Posted:
Sep 4, 2019
Last Verified:
Aug 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 4, 2019