Overview

Evaluation of Fenofibrate on Radiation-induced Skin Injury

Status:
Unknown status
Trial end date:
2020-04-13
Target enrollment:
0
Participant gender:
All
Summary
Fenofibrate is a specific ligand for PPARĪ±, which has been used for the treatment of hypercholesterolemia, hypertriglyceridemia, diabetes and cardiovascular diseases for long time. Fenofibrate reduces low-density lipoprotein (LDL), very low density lipoprotein (VLDL) and triglyceride levels, while increases high-density lipoprotein (HDL) levels. PPARĪ± has also shown antioxidant and anti-inflammatory properties. Fenofibrate confers cytoprotective effect against myocardial ischemia-reperfusion (I/R) injury in rats by suppressing cell apoptosis and ameliorates age-related renal injury through the activation of AMPK and SIRT1 signaling. However, the safety and effectiveness of fenofibrate on the progression of radiation-induced skin injury remain unknown. The purpose of this study is to determine whether topical application of fenofibrate is safe and effective for radiation-induced skin injury.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Second Affiliated Hospital of Soochow University
Treatments:
Fenofibrate
Criteria
Inclusion Criteria:

- Eligible patients had to have a pathologically proven cancer with a planned course of
radiotherapy.

- Normal haematological function (granulocyte count > 1.5 X 109 cells per litre,
platelet count > 100 X 109 cells per litre and haemoglobin > 100 g/L) and organ
function (creatinine clearance > 50 mL/min) and aspartate aminotransferase/alanine
aminotransferase < 2.5 of upper normal limit).

Exclusion Criteria:

- The presence of rash or unhealed wound in the radiation field, known allergy or
hypersensitivity to fenofibrate, pregnancy or lactation, history of/current connective
tissue disorder and prior radiation to the thorax.