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Chronic CholestasisNCT07569003

Prealbumin and IGF-1 Levels in Pediatric Chronic Cholestasis With Severe Malnutrition After Nutrition Therapy

A study testing Nutrition Therapy in people with Chronic Cholestasis and Severe Malnutrition, run by Universitas Indonesia at 1 site in Indonesia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to learn if a high-energy liquid diet improves the nutritional status of children with chronic cholestasis (a liver condition that blocks bile flow). Researchers want to see if this diet helps children who are malnourished. Read more about this study

Who is it for?
Ages Up to 5 years
What is being tested?
Nutrition Therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
1 siteIndonesia
Study dates
6 Apr 2026to Jul 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 5 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Children under 5 years old
  • Diagnosed with chronic cholestasis and severe malnutrition
  • Parental/guardian informed consent
  • Willingness to use a nasogastric tube (NGT) if indicated
  • Covered by national health insurance or other insurance

Who cannot join

  • Comorbidities (heart failure, chronic kidney disease, HIV)
  • Severe acute infections (acute gastroenteritis, dengue fever, pneumonia)
  • Post-liver transplant
  • Post-Kasai portoenterostomy (jaundice-free)
  • Currently exclusively breastfeeding
  • Use of steroids or NSAIDs within two weeks prior to the study.
  • Receiving a transfusion of whole blood, fresh frozen plasma, or platelets within one week prior to the study

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Tri Faranita, dr, Sp.A contact

+628126016641

tri.faranita@ui.ac.id

Klara Yuliarti, Dr. dr, Sp.A(K) contact

+628129300755

klarayuliarti@yahoo.com

Indonesia1 site, 1 recruiting
  • Faculty of Medicine, University of Indonesia, Jakarta, DKI Jakarta 10430

    Jakarta Pusat, DKI Jakarta, 10430

    Tri Faranita, dr., Sp.A, +628126016641, faranita.md@gmail.com

    Klara Yuliarti, Dr., dr., Sp.A(K), klarayuliarti@yahoo.com

    Recruiting

Other trials in Indonesia

About this study

Official title: Preliminary Study: Effect of Nutrition Therapy on Prealbumin and IGF-1 Level in Severe Malnutrition Under Five Years Old With Chronic Cholestasis

The goal of this clinical trial is to learn if a high-energy liquid diet improves the nutritional status of children with chronic cholestasis (a liver condition that blocks bile flow). Researchers want to see if this diet helps children who are malnourished.

The main questions the study aims to answer are:

Read more
  • Does the liquid diet raise the level of prealbumin (a marker of nutrition) in the blood?
  • Does the liquid diet raise the level of Insulin-like Growth Factor-1 (IGF-1) (a hormone that helps growth) in the blood?

Participants will:

  • Consume a high-energy liquid diet for 14 days.
  • Give blood samples at the start and at the end of the 2-week study.
  • Keep a daily record of what they eat and drink in a food diary. Researchers will compare the blood test results from the start and the end of the study to see if the liquid diet works to improve the children's prealbumin and IGF-1 levels. This study is important to help children with liver problems grow better and stay healthy.
Read the detailed description

The study evaluates the effect of nutritional therapy on prealbumin levels and insulin-like growth factor-1 (IGF-1) levels in malnourished children with chronic cholestasis aged 3-59 months (primary outcome) and diet tolerance, nutritional status, and medical condition (secondary outcomes).

Prealbumin and IGF-1 levels are measured as primary outcomes at baseline (day 0) and at day 15. Diet tolerance is assessed using the Bristol Stool Chart, a daily vomiting record throughout the 14-day intervention period, and allergic reactions. The frequency of defecation and consistency of each stool are documented. Allergic reactions are also monitored during the intervention period, including symptoms such as fever, erythematous rash, pruritus, and respiratory symptoms such as shortness of breath. The onset, duration, and severity of these symptoms are recorded.

Vomiting is evaluated as the number of episodes per day over the 14-day intervention period, and the volume of each episode is recorded. Only vomiting attributable to diet intolerance is included in the analysis, while episodes related to other causes, such as coughing or crying, are excluded.

Anthropometric parameters, including weight, height, mid-upper arm circumference, and other relevant measurements, are assessed on day 0, day 8, and day 15 to monitor changes in nutritional status.

Medical conditions during the study period are closely monitored, including underlying diseases, comorbidities, and intercurrent illnesses (e.g., respiratory or gastrointestinal infections). Clinical changes, hospitalizations, medication use, and any complications occurring during the intervention are recorded to evaluate their potential impact on nutritional status and study outcomes.

Nutritional therapy is administered as a liquid diet providing 130% of the recommended daily allowance (RDA), with macronutrient and micronutrient composition adjusted according to the 2019 ESPGHAN and 2021 Tessitore guidelines, over a 14-day intervention period. To ensure accurate nutritional intake, feeding is administered via a nasogastric tube, with gradual advancement of caloric intake until reaching 130% of RDA by day 4. Feeding is performed by parents or caregivers who are trained in proper administration techniques, feeding schedules, and hygiene practices. Monitoring of dietary adherence is conducted by daily food recall, instant messaging, and video call supervision during feeding sessions.

Protocol for nutritional therapy advancement is as follows:

  • Calorie requirement is calculated by multiplying ideal body weight with daily energy requirement (recommended dietary allowance, RDA).
  • Ideal body weight is defined as the median weight for actual height based on WHO growth charts (weight-for-height/length).
  • Height age is defined as the median age corresponding to the patient's actual height based on WHO growth charts (height/length-for-age).
  • The target energy intake is set at 130% of RDA according to height age, in line with ESPGHAN 2019 and Tessitore 2021 recommendations.
  1. On the first day: patients are provided with 44 to 140 more calories than their usual daily intake, based on the results of a food recall analysis. Nutritional therapy is administered as a liquid diet via a nasogastric tube, divided into 8 feeding sessions per day (every 3 hours).
  2. On the second day to fourth day: caloric intake is gradually increased until reaching 130% of RDA on the fourth day. The feeding regimen (volume and frequency) is adjusted according to patient tolerance.
  3. From fourth day to fourteenth day: the patient is maintained on full nutritional therapy at 130% of RDA. Monitoring of intake is conducted through daily food recall and communication via instant messaging/video calls.

Adjustments to feeding (volume, frequency, or rate) are made based on diet tolerance. If gastrointestinal intolerance or metabolic complications occur, nutritional therapy is modified according to clinical guidelines.

Being tested
Nutrition Therapy
Keywords
Chronic Cholestasis, Severe malnutrition, Pediatric cholestasis, IGF-1, Prealbumin, Nutrition therapy
Medical subject headings
Malnutrition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nutrition TherapyOther

    The nutritional therapy provided consists of a liquid formula with BPOM approval number MD 250976001600096 for subjects under 1 year of age, and BPOM approval number ML 562409102696 for subjects over 1 year of age. Patients are also given micronutrients in the form of vitamins A, D, E, and K, as well as vitamin B1, folic acid, and zinc as needed.

Study groups in NCT07569003
Study groupRoleWhat they receive
Nutrition Therapy GroupExperimentalNutrition therapy
Receives: Other: Nutrition Therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prealbumin and IGF-1 levels

    The difference in prealbumin and IGF-1 levels before and after 14 days of nutritional therapy

    Measured: 15 days

Secondary outcomes (8)
  1. Gastrointestinal tolerance for bowel movement

    Frequency of bowel movement per day and description of stool consistency (Bristol stool chart)

    Measured: 14 days

  2. Mid upper arm circumference changes

    Mid upper arm circumference changes is assessed using upper arm circumference measurements on the day of baseline and on the fifteenth day (after 14 days of nutritional intervention)

    Measured: 15 days

  3. Height gain

    Height gain is a change in height measured in centimetres with 1 decimal. The height gain is defined as the height on day 15 minus the height on day 0. Height on day 0 and day 15 will also be plotted on the WHO Growth Chart height-for-age z-score, and the change of height-for-age z-score will also be measured.

    Measured: 15 days

  4. Other illness duration

    Other illness duration refer to the duration of other illness (patient's illness unrelated to their primary illness) in days during the study.

    Measured: 14 days

  5. Gastrointestinal tolerance for vomit

    Frequency of vomit per day and volume of vomit

    Measured: 14 days

  6. Prevalence of allergic reaction

    Prevalence of subjects whom seems to have allergic reactions (rashes on skin) after receiving nutritional therapy

    Measured: 14 days

  7. Prevalence of vomiting

    Prevalence of participants experiencing vomiting after receiving nutrition therapy

    Measured: 14 days

  8. Prevalence of diarrhea

    Prevalence of participants experiencing diarrhea after receiving nutritional therapy

    Measured: 14 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2026
  2. Study start6 Apr 2026
  3. Primary completionJun 2026 (estimated)
  4. Study completionJul 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
Pre and post design
Masking
None (open label)
Enrolment
15 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07569003
Sponsor's protocol ID
25-12-1945
Status last verified
May 2026
First submitted
14 Apr 2026
Last updated
6 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Nutrition Therapy in people with Chronic Cholestasis and Severe Malnutrition, run by Universitas Indonesia at 1 site in Indonesia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Indonesia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Tri Faranita, dr, Sp.A (+628126016641, tri.faranita@ui.ac.id), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prealbumin and IGF-1 levels (time frame: 15 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2026.

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