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Trial · Interventional

CompletedPhase 3Results postedRegistry data

Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?

Overview

Status
Completed
Phase
Phase 3
Enrollment
100 participants (actual)
Sponsor
University of Virginia · Other
Design
Allocation not applicable · Open label (no masking)
Countries
1 country

United States

Start
29 Jan 2018
Primary completion
12 Mar 2019
Completion
12 Mar 2019
First posted
11 Dec 2017
Last update posted
9 Dec 2021
Conditions
Adrenal Insufficiency · Cirrhosis · Spur Cell Anemia · Lecithin Acyltransferase Deficiency

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
201820192020
  1. Ph 3

    Is Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?

    NCT03368066

    29 Jan 2018 to 12 Mar 2019

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The hepatoadrenal syndrome has been well described in the literature and is known to be associated with poorer outcomes in both stable and critically ill cirrhotic patients. In chronic liver disease, adrenal (and more specifically cortisol) insufficiency is thought to be a byproduct of altered lipid metabolism that results in decreased HDL production and thus decreased delivery of cholesterol to the adrenal for subsequent corticosteroid production. Studies to date have implicated lecithin-cholesterol acetyltransferase (LCAT) as the key enzyme which is deficient in some cirrhotic patients, leading to an impaired ability to esterify cholesterol and thus a loss of normal cellular functioning and membrane stability. The investigators seek to quantify this LCAT deficiency in a cohort of cirrhotic patients and demonstrate its association with various abnormal physiologies associated with chronic liver disease, including spur cell anemia, low HDL levels, and adrenal insufficiency. Hospitalized cirrhotic patients at UVA that meet study eligibility criteria will be approached by a member of the study team to obtain consent for participation. If a patient agrees to become a study subject, they will have an approximate total of 35ml of blood drawn the following morning. Lab tests to be performed include: peripheral blood smear, lipid panel, free cortisol, cortisol binding globulin, serum cholesterol esters (surrogate for LCAT enzyme activity), and a standard-dose cortisol stimulation test. The latter involves blood drawn with the initial collection, administration of an intravenous 250mcg dose of synthetic ACTH, and then repeat small-volume blood draws at 30 minutes and 60 minutes later. Subjects will be classified as adrenally sufficient or insufficient on the basis of as standard-dose cortisol stimulation test. Variables of interest for comparison between the groups include MELD score, Child-Turcotte-Pugh (CTP) classification, high-density lipoprotein (HDL) levels, presence of spur cell anemia, serum cholesterol ester percentage (surrogate for LCAT enzymatic activity), cortisol binding globulin levels, and free cortisol levels. Student's t-test and Chi Square tests will be utilized to determine significance; a p \<0.05 value will be used as our threshold for significance. If multiple factors are found to be significantly different in a univariate fashion between classification groups, a multivariate logistic regression analysis will be performed for adjusted analysis. The investigators will also seek to define any correlations between variables. Furthermore, the investigators will assess correlation between MELD score and serum cholesterol ester percentage, spur cell anemia, HDL levels, cortisol binding globulin levels, and free cortisol levels; similar correlate analysis will be done using CTP classification instead of MELD score.

Interventions

  • CosyntropinDrug

Arms1

  • Experimental

    Hospitalized cirrhosis patients

    Administration of cortisol stimulation test to assess for presence or absence of adrenal insufficiency

Primary outcomes3

Outcomes the sponsor listed as primary.

  1. Number of Participants With Cholesterol Esterification Deficiency

    Time frame · 24 hours

    Registry description

    A percent quantification of serum cholesterol esterification will be measured via blood draw. Low values represent deficiency in esterification, which is a surrogate measure of lecthicin-cholesterol acetyltransferase (LCAT) enzymatic deficiency.

  2. Number of Participants With Spur Cell Anemia

    Time frame · 24 hours

    Registry description

    A peripheral blood smear will be obtained and assessed for presence of acanthocytes (spur cells). Spur cell anemia is defined as a serum hemoglobin \< 10g/dL and the presence of \>= 5% spur cells on blood smear.

  3. Participant Transplant-Free Survival

    Time frame · 6 months

    Registry description

    Transplant and Death are considered equivalent outcomes

Secondary outcomes(8)
  1. Number of Participants With Relative Adrenal Insufficiency (RAI)

    Time frame · 24 hours

    Registry description

    A baseline total cortisol level will be obtained and then patients will receive a standard-dose synthetic ACTH (250mcg of Cosyntropin) stimulation test to assess for the presence of adrenal insufficiency. RAI is defined as a change in the total cortisol level in response to the stimulation test of \<9mcg/dL when measured 60 minutes after the Cosyntropin is administered.

  2. Number of Participants With Low Free Cortisol

    Time frame · 24 hours

    Registry description

    Patients will have their free cortisol levels measured to assess for deficiency.

  3. Number of Participants Who Received Liver Transplantation at 90 Days

    Time frame · 90 days

    Registry description

    Patients who received a liver transplant within 90 days of enrollment

  4. Number of Participants Who Received Liver Transplantation at 6 Months

    Time frame · 6 months

    Registry description

    Patients who received a liver transplant within 6 months of enrollment

  5. Number of Participants Who Died Within Index Hospitalization

    Time frame · Within Hospitalization

    Registry description

    Patients who died within the same hospitalization as enrollment

  6. Number of Participants Who Died at 30 Days

    Time frame · 30 days

    Registry description

    Patients who died within 30 days of enrollment

  7. Number of Participants Who Died at 90 Days

    Time frame · 90 days

    Registry description

    Patients who died within 90 days of enrollment

  8. Number of Participants Who Died at 6 Months

    Time frame · 6 months

    Registry description

    Patients who died within 6 months of enrollment

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeCount of participants· 24 hours

Number of Participants With Cholesterol Esterification Deficiency

GroupValue (Participants)
Normal Adrenal Response10
Relative Adrenal Insufficiency11
Primary outcomeCount of participants· 24 hours

Number of Participants With Spur Cell Anemia

GroupValue (Participants)
Normal Adrenal Response6
Relative Adrenal Insufficiency8
Primary outcomeCount of participants· 6 months

Participant Transplant-Free Survival

GroupValue (Participants)
Normal Adrenal Response41
Relative Adrenal Insufficiency16
Secondary and other outcome results(5)
Secondary outcomeCount of participants· 24 hours

Number of Participants With Relative Adrenal Insufficiency (RAI)

GroupValue (Participants)
Hospitalized Cirrhosis Patients37
Secondary outcomeCount of participants· 24 hours

Number of Participants With Low Free Cortisol

GroupValue (Participants)
Normal Adrenal Response6
Relative Adrenal Insufficiency1
Secondary outcomeCount of participants· 90 days

Number of Participants Who Received Liver Transplantation at 90 Days

GroupValue (Participants)
Normal Adrenal Response6
Relative Adrenal Insufficiency5
Secondary outcomeCount of participants· 6 months

Number of Participants Who Received Liver Transplantation at 6 Months

GroupValue (Participants)
Normal Adrenal Response8
Relative Adrenal Insufficiency6
Secondary outcomeCount of participants· Within Hospitalization

Number of Participants Who Died Within Index Hospitalization

GroupValue (Participants)
Normal Adrenal Response1
Relative Adrenal Insufficiency1

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Hospitalized Cirrhosis PatientsAdministration of cortisol stimulation test to assess for presence or absence of adrenal insufficiency Cosyntropin: Administer 250mcg cosyntropin to hospitalized cirrhosis patients to assess for the presence of adrenal insufficiency25 / 10025 / 1001 / 100

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies2

Studies that cite this trial.

More studies

2 studies on this page

PubMed tag: none · 2011

Assessment of adrenocortical reserve in stable patients with cirrhosis.

Fede et al. 2011Journal of hepatologycited by 61

PMID 21056503DOI 10.1016/j.jhep.2010.06.034PUB-21056503

Full text at the publisher
Publisher page

PubMed tag: none · 2010

Characterising adrenal function using directly measured plasma free cortisol in stable severe liver disease.

Tan et al. 2010Journal of hepatologycited by 66

PMID 20739086DOI 10.1016/j.jhep.2010.05.020PUB-20739086

Full text at the publisher
Publisher page

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 110 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Age \>=18 years * Diagnosis of cirrhosis * Admission to hospital Exclusion Criteria: * Age \< 18 years * Prior enrollment in study (i.e. readmission) * Prisoner * Pregnancy * Prednisone or Hydrocortisone use in last 24 hours

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