Evaluation of Lipoedema Tissue Transcriptome

Lipedema Clinical Trial

Official title:

Evaluation of Lipoedema Tissue Transcriptome

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05861583
• Other study ID #: Lipo2023
• Status: Recruiting
• Start date: January 1, 2023
• Est. completion date: March 1, 2024

Study information

• Verified date: July 2023
• Source: University Hospital Schleswig-Holstein
• Contact: Tobias Kisch, MD
• Phone: 004945150040512
• Email: tobias.kisch[@]uni-luebeck.de
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Lipoedema is a chronic painful disease with a fat distribution disorder affecting women. It is probably aggravated by hormonal changes. It is also discussed that a genetical predisposition might be a risk factor for developing lipoedema. The mechanisms leading to lipoedema are mostly unknown. The aim of this study is to identify molecular mechanisms and changes of the RNA-Expression pattern causing lipoedema by comparing the transcriptome of subcutaneous tissue of lipoedema patients vs. healthy subcutaneous tissue.

Description:

Lipoedema is a fat distribution disorder affecting mostly women. This chronic disease is characterized by painful fatty tissue accumulating especially at the limbs. The aetiopathogenesis of this disease is unsure. It is observed that a familial predisposition might increase the risk of developing lipoedema. Hormonal variations during puberty, pregnancy or climacteric period are also discussed as main factor for lipoedema. Molecular and genetical changes are rarely identified. The aim of this study is to identify changes in the expression pattern of fat cells causing lipoedema. One possibility to medicate this disease is to reduce the subcutaneous fatty tissue by liposuction. While this surgical procedure, a tumescent solution for reducing bleeding and pain is used. This study is also trying to identify the effect of tumescent solution to fatty tissue. This trial is an explorative study using excised tissue by surgery to compare the gene expression pattern of subcutaneous tissue of lipoedema patients to healthy subcutaneous tissue. Therefore, lipoedema patients of mild stage, moderate stage and severe stage as well as healthy patients with lipohypertrophy as control group are included to the study. The participation was on a voluntary basis. Only patients who reached the age of majority and who are able to consent were included. The study group patients are characterized by the typical, symmetrical and painful fat distribution especially at the limbs. The aim of the surgical treatment via liposuction of lipoedema patients is to reduce the fatty tissue, which is causing the development of oedema, the persistent pain and the formation of haematoma. The control group patients are determined by having a healthy subcutaneous fatty tissue, which was surgical reduced caused by cosmetical effects. The subcutaneous tissue therefore was reduced via liposuction following the standardised operation procedures. Starting the procedure, a small native tissue sample is collected without any additional invasive procedure. After installing a tumescent anaesthetic solution containing epinephrine and local anaesthetics subcutaneous the liposuction will be performed. The liposuction is done in power assisted liposuction technique. An additional sample of liposuctioned fat tissue treated with tumescent solution will be collected. The RNA-Expression pattern of the fatty tissue will be analysed by performing a NGS-Analysis. Changes of the RNA-Expression of lipoedema of different stages compared to normal fatty tissue will be detected. Further the effect of the intra-surgical used tumescent solution on fat cells can be detected by comparing native and treated tissue samples. Another aim of the study is to collect data concerning anamnestic aspects, symptoms and factors possibly leading to the development and progress of the disease. These data will be analysed to identify risk factors for lipoedema.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 80
• Est. completion date: March 1, 2024
• Est. primary completion date: December 1, 2023
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Lipohypertrophy: tissue from healthy patients (n=20): Consent-capable female patients =18 years of age with lipohypertrophy

2. Lipoedema milde stage: tissue from Lipoedema patients with mild stage 1 (n=20):

Consent-capable female patients =18 years of age with Lipoedema (Stage 1)

3. Lipoedema moderate stage: tissue from Lipoedema patients with moderate stage 2 (n=20):

Consent-capable female patients =18 years of age with Lipoedema (Stage 2)

4. Lipoedema severe stage: tissue from Lipoedema patients with severe stage 3 (n=20):

Consent-capable female patients =18 years of age with Lipoedema (Stage 3)

Exclusion Criteria:

• Inflammation in region of interest, HIV, Hepatitis

Related Conditions & MeSH terms

• Lipedema

Intervention

Other:
• fat tissue
fat tissue sample collected while cosmetical liposuction
• lipoedema tissue (stage 1)
lipoedema tissue sample (stage 1) collected while medical liposuction
• lipoedema tissue (stage 2)
lipoedema tissue sample (stage 2) collected while medical liposuction
• lipoedema tissue (stage 3)
lipoedema tissue sample (stage 3) collected while medical liposuction

Locations

Country	Name	City	State
Germany	University of Schleswig-Holstein	Lübeck	Schleswig-Holstein

Sponsors (3)

Lead Sponsor	Collaborator
University Hospital Schleswig-Holstein	Hanse-Klinik, Fachklinik für Liposuktion, Lübeck, Praxisklinik Kronshagen, Kiel-Kronshagen

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Differences in RNA-Expression pattern	Differences in RNA-Expression pattern between lipoedema tissue and lipohypertrophy tissue	1 day