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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02407769
Other study ID # GAS-1103-13/14-1
Secondary ID
Status Recruiting
Phase N/A
First received March 17, 2015
Last updated April 2, 2015
Start date February 2014
Est. completion date December 2017

Study information

Verified date March 2015
Source Universidad de Guanajuato
Contact Niko Alain Cruz Sancén
Phone 524661043578
Email nick_07a@hotmail.com
Is FDA regulated No
Health authority Mexico: Ministry of Health
Study type Interventional

Clinical Trial Summary

Assess the impact in body composition and handgrip strength of the nocturne supplementation by a month with BCAA (Enterex hepatic in patients awaiting liver transplantation)


Description:

Clinical trial study was make, data were obtained from people awaiting liver transplantation and with at least a criteria of protein/energy malnutrition (fase angle < 5.4°, subjective global assessment B or C and/or handgrip strength < 30 in men and < 20 in women). The investigators make them body composition assessment (weight, height, body mass index [BMI], mean arm circumference [MAC], muscle arm area [MAA], tricipital skinfold, Dual X ray absorptiometry [fat mass and fat free mass]) and handgrip strength at beginning and after 30 days of nocturne supplementation with BCAA and standardized diet (35-40 Kcal, 55% carbohydrates, 25% lipids and 20% proteins).


Recruitment information / eligibility

Status Recruiting
Enrollment 38
Est. completion date December 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients on waiting list for liver transplantation.

- Diagnosis of undernutrition.

Exclusion Criteria:

- Hepatorrenal syndrome.

- Hepatopulmonar syndrome

- Diabetes

- Overweight

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Late evening supplementation with branched chain amino acids
The patients will drink a Enterex Hepatic bag (500 Kcal, 18.6g of proteins of which 8.63g are branched chain amino acids, 71.7g of carbohydrates and 15.4g of lipids) during late evening (after 19:00 hours) in comparison with the late evening snack group which will eat a snack based in food with the next nutrimental facts (480 Kcal, 19g of proteins based in casein and vegetables sources, 17g of lipids and 63g of carbohydrates) during the same schedule that intervention group.

Locations

Country Name City State
Mexico Instituto Nacional de ciencias Médicas y Nutrición Salvador Zubirán México DF

Sponsors (2)

Lead Sponsor Collaborator
Universidad de Guanajuato 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 Change in Body Composition The body composition will be measured with air displacement pletismografy through Bodpod the results will be expressed in percentaje of fat mass and fat free mass. Basal and 30 and 60 days after intervention. Yes
Secondary Change in Mid arm muscle area Estimation of muscle area of the no dominant arm using the formula [(MAMA - (p x PT))2 / 4 p ]
- 10 in men and -6.5 in women, the result is expressed in cm2.
Basal and 30 and 60 days after intervention. Yes
Secondary Change in Quality of life It will be measured by the questionnaire SF-36 that is a generic scale providing a health profile and is applicable for both, patients and general population; the results that the 36 questions divided in 8 dimensions. The patients answers will be transformed to a numeric scale: since 0 (worst) to 100 (better) Basal and 30 and 60 days after intervention. Yes
Secondary Change in Fase angle. vectorial sum of the resistance and reactance result in the impedance, and the angle that is formed is called the fase angle; this is obtain through a impedanciometre, the measure is expressed in grades. Basal and 30 and 60 days after intervention. Yes
Secondary Change in Handgrip strength. Handgrip strength of the no dominant hand will be measured by a hand dynamometer in kilograms/Force Basal and 30 and 60 days after intervention. Yes
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