Fact CheckerSign in

NCT07315022CompletedPhase 4

Enhanced Recovery After Surgery-Based Multimodal Preemptive Analgesia for Perioperative Management in Transarterial Chemoembolization of Intermediate-to-Advanced Hepatocellular Carcinoma

Enhanced Recovery After Surgery-Based Multimodal Preemptive Analgesia for Perioperative Management in Transarterial Chemoembolization of Intermediate-to-Advanced Hepatocellular Carcinoma: a Multicenter Retrospective Cohort Study

Source: ClinicalTrials.gov · Last updated 2 Jan 2026

Brief summary (registry, in English)

To evaluate the effectiveness of the combination of hydrochloride hydromorphone and flurbiprofen ester for post-TACE intravenous patient-controlled intravenous analgesia (PCIA).

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
129 (actual)
First submitted
5 Dec 2025
Start date
1 Aug 2024
Primary completion date
30 Aug 2025
Lead sponsor
First Affiliated Hospital, Sun Yat-Sen University
NCT number
NCT07315022

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 129
  • From 1 Aug 2024 to the primary completion date, 30 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of iodine contrast allergy;
  • severe psychological or psychiatric disorders;
  • history of long-term analgesic medication use;
  • severe cardiopulmonary disease;
  • severe uncontrolled infection;

Other

  • incomplete medical records.

Who the study is looking for

  • Pathologically or clinically diagnosed with hepatocellular carcinoma according to the "Guidelines for Diagnosis and Treatment of Primary Liver Cancer" issued by the National Health Commission of China in 2024;
  • staged as China Liver Cancer Stage II-III1 or 2022 Barcelona Clinic Liver Cancer stage B-C14;
  • liver function classified as Child-Pugh grade A or B;
  • ECOG PS score 0-215;
  • meeting the following hematological criteria: white blood cell count ≥3×10⁹/L, platelet count ≥50×10⁹/L, hemoglobin ≥80 g/L, serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) ≤twice the upper limit of normal (ULN), serum creatinine ≤1.5×ULN, INR \<1.5 or prothrombin time \<ULN + 4 s, albumin (ALB) ≥30 g/L, total bilirubin \<34 mmol/L.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital, Sun Yat-sen University
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.