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Active, not recruitingNCT05935800Updated Jun 10, 2026

The Effect of the COVID-19 Pandemic on Frailty in Liver Transplant Candidates

An observational study in Frailty, Sarcopenia and COVID-19, sponsored by Methodist Health System. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-06-10.

Sponsored by Methodist Health System · Observational

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Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
208
Ages
18 Years to 75 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 185 studies in Frailty with a site in United States — 50 open to participants now, 62 under way, 1 of them phase 3. Frailty · United States.

Planned enrollment
19th of 42
208 · median 128
Started
2022
with 18 others
Observational
42 of 185
10 open now
Primary completion
2027-04
later than 38 of 60 live
Registered
140th of 185
by date

Among the 185 studies in Frailty with a site in United States, this one is the 19th largest by planned enrollment of the 42 observational ones that give a count, is one of 19 that started in 2022, is one of 42 observational ones, reaches primary completion later than 38 of the 60 other live ones, and was the 140th registered.

Frailty

1,284 studies on the registry are indexed under Frailty; 451 are open to participants now.

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Open to participants now

50 of the 185 studies in Frailty with a site in United States are open now. Recruiting first, the newest first:

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All 50 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 299 Frailty studies recruiting now, 235 (79%) set no upper age limit and 9 (3%) stop at 75 or younger; 7 take children under 18; 66 take healthy volunteers.

This study: 18 Years to 75 Years · all sexes · no healthy volunteers.

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02

Study summary

Frailty is associated with higher rates of morbidity, mortality, and failure to rescue after major surgical procedures. Sarcopenia is degenerative loss of skeletal muscle mass and strength. It is a key component of physical frailty and is associated with poorer post-surgical outcomes due to decreased patient strength and vitality.

Read the detailed description

This study seeks to examine whether the (COVID-19) pandemic, an ongoing global health crisis that was declared a national emergency by the US Federal Government on March 13, 2020, has exacerbated both frailty and sarcopenia in a population of liver transplant candidates.

03

Conditions studied

  • Frailty
  • Sarcopenia
  • COVID-19
04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Age 18 years and older Underwent pre-transplant frailty assessment (PFA) at MDMC 369 liver transplant candidates who underwent pre-transplant frailty assessments at the Liver Institute at Methodist Dallas from April 1, 2018 to February 28, 2022. The study data will be divided into cohorts: pre-COVID and COVID. Specifically, the pre-COVID period will consist of the dates between April 1st, 2018 and March 12, 2020, while the COVID period will consist of the dates between March 13, 2020 and February 28th, 2022.

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Inclusion criteria

  • Age 18 years and older Underwent pre-transplant frailty assessment (PFA) at MDMC

Exclusion criteria

Exclusion Criteria:

  • Not a patient at Liver Institute at Methodist Dallas
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
208 participants (estimated)
Patient registry
No

Interventions

  • BehavioralCOVID Patients who Underwent pre-transplant frailty assessment (PFA) at MDMC

    This is a single-center, retrospective study that uses de-identified, anonymized patient data. Data from 369 liver transplant candidates who underwent pre-transplant frailty assessments at the Liver Institute at Methodist Dallas from April 1, 2018 to February 28, 2022. The study data will be divided into cohorts: pre-COVID and COVID. Specifically, the pre-COVID period will consist of the dates between April 1st, 2018 and March 12, 2020, while the COVID period will consist of the dates between March 13, 2020 and February 28th, 2022.

06

What researchers measure

Primary outcomes

  1. To determine the impact of the COVID-19 pandemic on the prevalence of sarcopenia

    To determine the impact of the COVID-19 pandemic on the prevalence of sarcopenia and frailty in patients undergoing liver transplant evaluation at Methodist Dallas Medical Center

    Time frame: 2 years

  2. To determine the impact of the COVID-19 pandemic on the incidence of sarcopenia

    To determine the impact of the COVID-19 pandemic on the incidence of sarcopenia and frailty in patients undergoing liver transplant evaluation at Methodist Dallas Medical Center

    Time frame: 2 years

Secondary outcomes

  1. Changes in number of comorbidities between pre- and during/post-pandemic periods

    Changes in number of comorbidities between pre- and during/post-pandemic periods

    Time frame: 1 year

  2. Changes in type of comorbidities between pre- and during/post-pandemic periods

    Changes in type of comorbidities between pre- and during/post-pandemic periods

    Time frame: 1 year

  3. Changes in severity of comorbidities between pre- and during/post-pandemic periods

    Changes in severity of comorbidities between pre- and during/post-pandemic periods

    Time frame: 1 year

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Apr 2022 (actual). Primary completion is estimated for Apr 2027, 60 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 6, 2023
First posted
Jul 7, 2023
StartActual
Apr 19, 2022
Primary completionEst.
Apr 19, 2027
CompletionEst.
Apr 19, 2028
Last update
Jun 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05935800
Responsible party
Sponsor
First posted
Jul 7, 2023
Start date
Apr 19, 2022
Primary completion
Apr 19, 2027 (estimated)
Completion
Apr 19, 2028 (estimated)
Last update
Jun 10, 2026

Study contacts

Parvez Mantry, MD
principal investigator · Methodist Health System

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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