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the Effect of Nutrition-optimized Prehabilitation on Perioperative Intervention in Primary Liver Carcinoma

StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Primary endpoint(s) modified Show 11 more changesShow less
    • Trial completed
    • Final enrollment: 132 participants (planned 120)
    • Study completion date changed from estimate of Oct 31, 2026 to Sep 29, 2026
    • Study sites: 1 to 3
    • Primary completion date changed from estimate of Sep 30, 2026 to Sep 1, 2026
    • Start date: Sep 1, 2024 to May 10, 2024
    • Secondary endpoints revised (4)
    • Study description shortened, about 75 words
    • Collaborators revised (2)
    • Publications: details revised at 5 of 5 entries
    • Eligibility criteria expanded, about 5 words
  2. Enrollment target: 200 to 120v3 Show 8 more changesShow less
    • Primary completion date: Dec 31, 2025 to Sep 30, 2026
    • Primary endpoints: 3 to 1
    • Study completion date: Jan 31, 2026 to Oct 31, 2026
    • Eligibility criteria shortened, about 23 words
    • Secondary endpoints: 5 to 4
    • Study description shortened, about 40 words
    • Collaborators expanded, about 6 words
    • Study title revised
  3. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Study sites: 0 to 1
    • Primary completion date: Nov 2025 to Dec 31, 2025
    • Study completion date: Jan 2026 to Jan 31, 2026
    • Start date changed from estimate of Sep 2024 to Sep 1, 2024
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The aim of this project is to investigate the effect of triple prehabilitation led by nutritional optimization in liver cancer patients' surgery. It improves the preoperative nutritional status of cancer patients, reduces the incidence of early postoperative complications, promotes postoperative recovery, and improves the quality of patients' survival. Patients were randomized into experimental and control groups based on exclusion and inclusion criteria. Both groups received exercise and psychological interventions; for nutritional intervention, the experimental group received an ordinary diet plus oral nutritional supplementation, whereas the control group received an ordinary diet alone. Routine clinical blood tests will be performed at the time of enrollment, on the first day before surgery and on the first, third and fifth days after surgery. Enrolled patients were followed up by telephone or outpatient clinic at 1 month postoperatively.
Trial Details
NCT Number NCT06549829
Lead Sponsor Second Affiliated Hospital, Zhejiang University, School of Medicine
Collaborators: Shangrao People's Hospital, Huzhou Central Hospital
Conditions
(from sponsor)		 Hepatocellular Carcinoma, Liver Carcinoma, Hepatobiliary Cancers, Primary Liver Cancer
Related terms Carcinoma, Hepatocellular
Enrollment 132 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov