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The Effect of Late-evening Snacks on Patients With Primary Hepatocellular Carcinoma After Hepatectomy

Effects of Late-evening Snacks on Nutritional Status and Metabolic Pattern of Patients With Primary Hepatocellular Carcinoma After Hepatectomy

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06278701
Enrollment
106
Registered
2024-02-26
Start date
2023-11-01
Completion date
2025-07-30
Last updated
2024-02-26

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

Conditions

Liver Neoplasms

Keywords

Liver cancer, late evening snack, Metabolic pattern, Nutritional status

Brief summary

Late-evening snacks, in which a portion of food is moved to bedtime while the total amount of food eaten per day remains unchanged, can effectively improve the metabolic state of accelerated catabolism. The goal of this clinical trial is to learn about the effects of late-evening snacks on health conditions of hepatocellular carcinoma patients who underwent hepatectomy, and to further explore the effects of late-evening snacks on patients' metabolic patterns. The main question it aims to answer are: • the effect of late-evening snacks on the nutritional status of hepatic resection patients with hepatocellular carcinoma; * the effect of late-evening snacks on the recovery of liver function in liver cancer hepatectomy patients; * the effect of late-evening snacks on the complication rate of hepatic resection patients with hepatocellular carcinoma; * the effect of late-evening snacks on long-term quality of life of hepatic resection patients with hepatocellular carcinoma; * the effect of late-evening snacks on the metabolic pattern of hepatic resection patients with hepatocellular carcinoma. After learning about the 2 dietary modalities of the late-evening snacks and regular diet, patients will be placed in the different groups according to your preference. Patients who enter the test group will have additional meal 1h before bedtime every day, while patients in the control group will have normal diet. Patients will be asked to : * eat 1h before bedtime; * follow the doctor's instructions during their stay in the hospital; * have follow-up examinations at 1 month, 3 months and 6 months after the operation, after which blood samples will be collected for metabolite testing.

Interventions

OTHERlate-evening snacks

have an additional meal 1h before bedtime (total calories 200-275kcal, protein 11.5g-18g, complex carbohydrates 25-55g).

Sponsors

DU Yao
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This study utilizes a grouping method based on patient preference. You will learn about the 2 dietary modalities, the late-evening snacks and the regular diet, and then you will be placed in the different groups according to your preference. Patients who volunteer for the 1h bedtime meal will be in the test group and those who volunteer for the regular diet will be in the control group. Dietary counseling and follow-up visits will be conducted in both groups, the difference being the presence or absence of the 1h bedtime meal pattern.

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-75 years; * Meet the diagnostic criteria of China's Guidelines for Diagnosis and Treatment of Primary Liver Cancer (2022 Edition), clinically diagnosed with primary liver cancer, hospitalized with radical hepatectomy as the main surgical treatment, no indication of metastasis of the tumor to extra-hepatic organs in preoperative tests and examinations, no absolute contraindications to surgery, complete resection of the liver tumor in the operation, and hepatocellular carcinoma confirmed by postoperative pathological diagnosis; * Child-Pugh grades A and B; * Preoperative Eastern Cooperative Oncology Group Physical Status Score (ECOG-PS) of 0 to 2; * The patient is conscious, has normal verbal communication, and is able to cooperate with the relevant examinations; * Fully informed about the study and voluntarily signed an informed consent form.

Exclusion criteria

* Failure to meet selection criteria; * Nutritional assessment as cachexia; * Presence of contraindications to enteral nutrition (EN) or EN intolerance, such as acute gastrointestinal bleeding, intestinal obstruction.(≥ grade 3, National Cancer Institute-Common Terminology Criteria for Adverse Events \[NCINCI-CTCAE v 5.0\]); * Simultaneous combination of malignant tumors in other parts of the body; * Combined hepatic encephalopathy or definite infection on admission; * Known refractory metabolic diseases (e.g., poorly controlled diabetes mellitus or fasting glucose ≥10 mmol/L, hyperthyroidism, hypothyroidism, metabolic acidosis); * Decreased renal function (defined as serum creatinine Cr level ≥176.8 μmol/L); * Intravenous or oral nutritional supplements, such as proteins, amino acids, etc., applied within one month prior to admission to the hospital; * Patients with severe stress or severe complications such as respiratory failure with severe cardiac, hepatic, renal and other insufficiencies; * Persons with mental and neurological disorders who are unable to cooperate with a physician; * Alzheimer's disease, cerebral atrophy, acute stage or sequelae of cerebrovascular disease, cognitive impairment; * Previously poor adherence to medication and nutritional counseling; * Critically ill and difficult to assess; * On the liver transplant waiting list or under consideration for liver transplantation, as such patients may discontinue follow-up before the end of the study; * Less than 12 months since last localized treatment (TACE or HAIC or ablative therapy); * Other circumstances that the researcher considers inappropriate for participation in the study.

Design outcomes

Primary

MeasureTime frameDescription
Albumin risingDay 1 of admission/Post-operative day 6/1 month postoperative/3 months postoperative/6 months postoperativeSerum albumin levels in patients at each time point

Secondary

MeasureTime frameDescription
Decrease in CholinesteraseDay 1 of admission/Post-operative day 6/1 month postoperative/3 months postoperative/6 months postoperativeSerum levels of cholinesterase in patients at each time point
Prealbumin risingDay 1 of admission/Post-operative day 6/1 month postoperative/3 months postoperative/6 months postoperativeSerum levels of prealbumin in patients at each time point
Decrease in Alanine AminotransferaseDay 1 of admission/Post-operative day 6/1 month postoperative/3 months postoperative/6 months postoperativeSerum levels of alanine aminotransferase in patients at each time point
Decrease in Aspartate AminotransferaseDay 1 of admission/Post-operative day 6/1 month postoperative/3 months postoperative/6 months postoperativeSerum levels of aspartate aminotransferase in patients at each time point
Lower total hospitalization costsFrom admission to discharge,an average of 1 monthTotal cost from patient hospitalization to discharge
Relapse-Free SurvivalFrom the time the patient underwent hepatectomy until the date of first recording to the date of progression or death from any cause, whichever comes first, assessed up to 2 yearsTime from when the patient achieved complete remission after hepatectomy to the time of recurrence or cutoff for follow-up
Improved quality of life1 month postoperative/3 months postoperative/6 months postoperativePatients completed EORTC QLQ-C30 at various time points
Decrease in Total bilirubinDay 1 of admission/Post-operative day 6/1 month postoperative/3 months postoperative/6 months postoperativeSerum levels of total bilirubin in patients at each time point

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026