跳至主要内容
临床试验/NCT05629026
NCT05629026招募中不适用

Study of Lymphatic Dysfunction in Primary and Secondary Lymphedema

University Hospital, Toulouse1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年2月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Number of RNA transcripts between lymphoedema limb and healthy limb

研究概览

简要总结

Lymphedema is a disorder of the lymphatic vascular system characterized by impaired lymphatic return and swelling of the extremities and accumulation of undrained interstitial fluid/lymph that results in fibrosis and adipose tissue deposition in the affected area. It can be an inherited condition (primary lymphedema) or occurs after cancer surgery and lymph node removal (secondary lymphedema). It causes a significant morbidity and is a common disabling disease affecting more than 200 million people worldwide, however there is no curative treatment for primary or secondary lymphedema.

详细描述

Primary lymphedema is an inherited condition whereas secondary lymphedema develops after cancer treatments. Despite common phenotype, a molecular and histological comparison of these two pathologies has never been performed. Primary lymphedema is associated with heterozygous inactivating mutations of the gene encoding vascular endothelial growth factor C and D receptor (VEGFR-3). Primary lymphedema is rare, affecting 1 in 100,000 individuals. Secondary lymphedema is the most common cause of the disease and affects more than 200 million people worldwide.

Secondary lymphedema occurs months, sometimes years after cancer surgery suggesting that lymphedema is not only a side effect of the surgery, but involves modifications of the lymphatic architecture as well as its microenvironment, in particular adipose tissue that accumulates in the limb.

There is no cure for lymphedema because of the lack of identified therapeutic strategies able to restore collecting lymphatic draining function in the arm or in the leg. The goal will be to establish if these pathologies which possess a common denomination exhibit a similar gene expression.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients in who developed primary lymphedema or secondary lymphedema after breast cancer treatment.
  • •Male and female over the age of 18 and under
  • •Patient affiliated to a social security scheme in France.
  • •Patient having signed informed consent prior to inclusion in the study and prior to any specific procedure for the study.
  • •Patients with no recidive > 3 years after cancer surgery.
  • •Patients with Body Mass Index <
  • •Patient enrolled in a care pathway for the management of their lymphedema (medical and educational care).
  • •Patients wearing a compression orthosis on the limb with lymphedema.

排除标准

  • •Patients with strong suspicion or with active bacterial or fungal infection.
  • •Patient with venous insufficiency associated with lymphedema.
  • •Patient with a history of deep venous thrombosis on the limb with lymphedema.
  • •History of chronic inflammatory disease.
  • •Active neoplasia during parallel management.
  • •Patient already included in another therapeutic trial.
  • •Pregnant or breastfeeding woman.
  • •Metastatic cancer.
  • •Bilateral breast cancer.
  • •Obliterative arterial disease.
  • •Multiple erysipelas.
  • •Active smoking (delayed healing).
  • •Medicines that may promote delayed healing (Corticosteroid therapy, immunosuppressants).
  • •Medication that thins the blood (aspirin and antiplatelet agent, anti-coagulant).
  • •Betadine allergy.
  • •Patient under guardianship or trusteeship, persons placed under the protection of justice

研究组 & 干预措施

primary lymphoedema

Experimental

patients with primary lymphoedema

干预措施: Micro-biopsies (Procedure)

secondary lymphoedema

Experimental

patients with secondary lymphoedema

干预措施: Micro-biopsies (Procedure)

结局指标

主要结局

Number of RNA transcripts between lymphoedema limb and healthy limb

时间窗: Day 1

The gene expression profile of primary and secondary lymphedema will be determined by high-throughput RNA sequencing (RNAseq) or next-generation sequencing (NGS). It is a molecular methodology that allows the rapid sequencing of thousands to millions of RNA molecules simultaneously, determining the unique and specific order of nucleic acid bases. It is a random sequencing of the whole transcriptome which is used to identify and quantify the RNA resulting from the transcription of the genome at a given time.

次要结局

  • LYVE-1 expression in primary and secondary lymphedema by immuno-histology(Day 1)
  • Podoplanin expression in primary and secondary lymphedema by immuno-histology(Day 1)
  • Chromatography analysis of Lipids in adipose tissues from primary and secondary lymphoedema(Day 1)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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