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Diet and children with chronic liver disease

The effect of nutritional modification program on quality of life and liver-specific symptoms in children with chronic liver disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015091424019N1
Enrollment
75
Registered
2016-01-30
Start date
2014-06-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic Liver Disease. Liver disease, unspecified

Interventions

Intervention 1: Training was conducted in 6 sessions. In the first two sessions, which were the subject of meetings liver disease, and its impact on nutrition. 4 other meeting issues of energy consump
Training was conducted in 6 sessions. In the first two sessions, which were the subject of meetings liver disease, and its impact on nutrition. 4 other meeting issues of energy consumption, carbohydra
Training was conducted over 2 sessions. Which were the subject of meetings liver disease, and its impact on nutrition

Sponsors

Department of Science and Technology of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for children: 1. Children with liver disease who are at least 6 months old disease 2. Iranian citizenship is a lie Mashhad. 3. patients tend to have the company study. 4. phone calls possible. 5. Children with chronic liver disease have other physical limitations. 6. children with chronic liver disease, mental health is not restricted. 7. aged 2 to 18 years old. Exclusion criteria related to children: 1. there is no desire to continue cooperation. 2. children to be fed TPN. 3. Children need to have a feeding tube. Inclusion criteria for the appropriate care: 1. The desire to have the company study. 2. Help is at least the third degree. 3 phone calls possible. Exclusion criteria for the appropriate care: 1. Randashth workshop is willing to continue cooperating companies

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: First and end of the study. Method of measurement: Questionnaire Peds ql 4.0.;Prothrombin time. Timepoint: First and end of the study. Method of measurement: Values obtained from tests of Biochemistry.;Albumin. Timepoint: First and end of the study. Method of measurement: Values obtained from tests of Biochemistry.;Bilirubin. Timepoint: First and end of the study. Method of measurement: Values obtained from tests of Biochemistry.;Aspartate aminotransferase. Timepoint: First and end of the study. Method of measurement: Values obtained from tests of blood.;Alanine amino transferase. Timepoint: First and end of the study. Method of measurement: Values obtained from tests of blood.

Secondary

MeasureTime frame
Height. Timepoint: First and end of the study. Method of measurement: The value of the stadiometer.;Weight. Timepoint: First and end of the study. Method of measurement: The value of the bio-electrical impedance devices.;Body Mass Index. Timepoint: First and end of the study. Method of measurement: Body weight divided by the square of Height is achieved Index.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactzahra namjou

Mashhad University of Medical Sciences

z.namjou@yahoo.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026