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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02023190
Other study ID # LT01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 3, 2019
Est. completion date December 2022

Study information

Verified date February 2020
Source Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Contact Aldo Torre, MD MSci
Phone 54870900
Email detoal@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 2022
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Liver cirrhosis (any etiology)

- Enrolled in waiting list for tliver transplant

Exclusion Criteria:

- Hepatocellular carcinoma

- Chronic renal failure

- Congestive cardiac failure

- Extremity amputation

- Pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Mexico Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran Mexico City DF

Sponsors (1)

Lead Sponsor Collaborator
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Body composition Body composition will be assessed through bioelectrical impedance vector analysis graph. Baseline, 7 days, 1 month, 3 months and 6 months post-tranpslant
Secondary Liver function tests Baseline, 7 days, 1 month, 3 months and 6 months post-tranpslant
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