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Outcomes Using MARS for Patients With ALF

Outcomes Using MARS: A Single Center Experience

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05594953
Enrollment
27
Registered
2022-10-26
Start date
2021-04-23
Completion date
2026-05-12
Last updated
2026-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Liver Failure, Alcoholic Hepatitis

Brief summary

Retrospective chart review will be conducted on patients at Methodist Dallas Medical Center, meeting the inclusion criteria from January 1, 2019 to December 15, 2020 to determine the transplant free survival and overall survival and other secondary outcome measures.

Detailed description

Retrospective chart review will be conducted on patients at Methodist Dallas Medical Center, meeting the inclusion criteria from January 1, 2019 to December 15, 2020 to determine the transplant free survival and overall survival and other secondary outcome measures. Patient's charts will be accessed on EPIC by the PI or delegated study personnel. The investigator's anticipate completion of this study by January 31, 2022.

Interventions

None listed

Sponsors

Methodist Health System
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

• The patient was diagnosed with: Alcoholic hepatitis; AoCLF; OR Acute fulminant liver failure • The patient underwent at least one round of dialysis using plasma exchange or MARSTM

Exclusion criteria

* Patient not meeting the inclusion criteria will be excluded. All patients who underwent MARS at MDMC will be included in the study population.

Design outcomes

Primary

MeasureTime frameDescription
Transplant free survival mortalityRate at 30 daystransplant will be measured by date of death, and discharge
Difference in DemographicsRate at 30 daysco-morbidities, etiology of liver failure between those treated with MARS vs. controls
Improvement in TransplantRate at 30 daysDetermine whether treatment with MARS can help facilitate improvement in HE, LOS, and ICU duration.

Secondary

MeasureTime frameDescription
DemographicsJanuary 1, 2019 to January 31, 2022age (years), gender (male/female), race (Caucasian, black, Hispanic, Asian, other), BMI (kg/m2)
Hepatorenal syndrome(in hospital [date of death or discharge or transplant]) and at 30 daysY/N
Need for vasopressor support(in hospital [date of death or discharge or transplant]) and at 30 daysY/N
Sepsis (as measured by by QSOFA criteria):(in hospital [date of death or discharge or transplant]) and at 30 daysY/N
Need for CRRT as documented in the chart:(in hospital [date of death or discharge or transplant]) and at 30 daysY/N
ICU durationdate of ICU admission and date of discharge (or death)days of date of ICU duration
long term dialysis(in hospital [date of death or discharge or transplant]) and at 30 daysNeed for long term dialysis (Y/N)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORParvez Mantry, MD

Methodist

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026