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NCT06864221Recruiting

Plasma Sphingolipid Metabolites and Radiotherapy Efficacy in Hepatocellular Carcinoma

Correlation Between Plasma Sphingolipid Metabolites and the Efficacy of Radiotherapy in Hepatocellular Carcinoma

Source: ClinicalTrials.gov · Last updated 12 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Plasma contains a variety of metabolites, among which sphingolipids, including ceramide, sphingosine, and sphingosine-1-phosphate, serve as important intracellular second messengers and are involved in various cellular signaling pathways, such as apoptosis. We hypothesize that plasma sphingolipid levels may be associated with the efficacy of radiotherapy for liver cancer. This study will utilize LC-MS/MS technology for qualitative and quantitative analysis of plasma sphingolipids in liver cancer patients undergoing radiotherapy. Clinical data related to patient prognosis will also be collected to investigate the correlation between plasma sphingolipid levels and the therapeutic efficacy of liver cancer radiotherapy. The aim is to establish the clinical diagnostic significance of plasma sphingolipid levels in predicting the efficacy of liver cancer radiotherapy, providing new insights to enhance the effectiveness of radiotherapy in liver cancer treatment.

Status (registry)
Recruiting
Study type
Observational
Enrollment
260 (estimated)
First submitted
3 Mar 2025
Start date
1 Sept 2024
Primary completion date
1 Jan 2026
Lead sponsor
Nanfang Hospital, Southern Medical University
NCT number
NCT06864221

What you commit to

  • Study type: Observational
  • Planned participants: 260
  • From 1 Sept 2024 to the primary completion date, 1 Jan 2026
  • 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.

Prior treatment

  • Patients who discontinued radiotherapy or did not complete the planned treatment.

Other illness

  • Presence of malignancies from other origins.
  • Severe metabolic diseases such as uncontrolled diabetes, significant obesity, or fatty liver disease.
  • Uncontrolled comorbidities, such as severe cardiovascular or pulmonary diseases, that may affect treatment or study outcomes.

Who the study is looking for

  • Patients voluntarily signed the informed consent form.
  • Aged between 18 and 80 years.
  • Clinically diagnosed with primary liver cancer according to the latest treatment guidelines.
  • Determined by the treating physician to require radiotherapy.
  • Expected survival time of more than 3 months.

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
Nanfang Hospital, Southern Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

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