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Status unknownNCT02023190Updated Mar 2, 2020

Changes in Body Composition and Nutritional Status in Patients Undergoing Liver Transplantation

An observational study in Liver Cirrhosis, sponsored by Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran. Status unknown at 1 site in Mexico. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2020-03-02.

Sponsored by Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran · Observational

The sponsor has not verified this record recently (last verified Feb 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
18 Years to 60 Years
Sex
All
01

Study summary

Liver transplant is the goal treatment for every patient with end-stage chronic liver disease.

Quality of life improves after transplant because the main complications of end-stage liver disease disappear, but due to immunosuppression other alterations appear such as metabolic alterations, weight gain, among others.

Body composition and nutritional status can be affected do to post-transplant pharmacologic therapy.

Read the detailed description

Body composition and nutritional status can be affected due to post-transplant pharmacologic therapy.

This is a prospective cohort study, patients from liver transplant waiting list will be assessed, pre and post-transplant measures of body composition and nutritional status will be obtained.

02

Conditions studied

  • Liver Cirrhosis

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Keywords

  • liver cirrhosis
  • liver transplant
  • nutritional status
  • bioelectrical impedance vector analysis
03

In context

Liver Cirrhosis

1,668 studies on the registry are indexed under Liver Cirrhosis; 360 are open to participants now.

This study's planned enrollment of 60 is below the median of 152 across 605 observational studies indexed under Liver Cirrhosis.

Browse Liver Cirrhosis studies →

Lead sponsor

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran is the lead sponsor of 144 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients will be selected from the transplant enrollment list at the Department of Gastroenterology in a tertiary care center in Mexico

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Liver cirrhosis (any etiology)
  • Enrolled in waiting list for tliver transplant

Exclusion criteria

Exclusion Criteria:

  • Hepatocellular carcinoma
  • Chronic renal failure
  • Congestive cardiac failure
  • Extremity amputation
  • Pregnancy
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No

Groups and cohorts

  • Nutritional assessment

    Nutritional assessment will be performed by bioelectrical impedance vector analysis

06

What researchers measure

Primary outcomes

  1. Body composition

    Body composition will be assessed through bioelectrical impedance vector analysis graph.

    Time frame: Baseline, 7 days, 1 month, 3 months and 6 months post-tranpslant

Secondary outcomes

  1. Liver function tests

    Time frame: Baseline, 7 days, 1 month, 3 months and 6 months post-tranpslant

07

Study locations

1 of 1 sites recruiting
  • Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
    Mexico City, Mexico City 14000, Mexico
    • Aldo Torre, MD MSci · Contact · detoal@yahoo.com · 54870900
    • Astrid Ruiz-Margain, M.Sci · Contact · ruizm.astrid@gmail.com · 54870900
    • Aldo Torre, MD MSci · Principal investigator
    • Astrid Ruiz-Margain, M.Sci · Principal investigator
    • Ricardo U Macias-Rodriguez, MD MSci · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 2, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02023190
Responsible party
ALDO TORRE DELGADILLO (Principal investigator, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran) — Principal investigator
First posted
Dec 30, 2013
Start date
Jan 3, 2019
Primary completion
Dec 2020 (estimated)
Completion
Dec 2022 (estimated)
Last update
Mar 2, 2020

Study contacts

Aldo Torre, MD MSci
Contact
detoal@yahoo.com
54870900 ext. 2711
Astrid Ruiz-Margain, M.Sci
Contact
ruizm.astrid@gmail.com
54870900 ext. 2711
Aldo Torre, MD MSci
study chair · Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Astrid Ruiz-Margáin, M.Sci
principal investigator · Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

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