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TuLip : Role of the Tumor Environment in Cancer-related Fat Loss

U

Université Catholique de Louvain

Status

Terminated

Conditions

Cachexia
Cancer
Adipose Tissue

Treatments

Procedure: Nissen Fundoplication, cholecystectomy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Cancer cachexia is defined as a weight loss of more than 5% over the last 6 months, a loss of body fat and muscle atrophy. It is found in 80% of patients with advanced cancer. In this context, white adipose tissue is a particularly interesting target since its depletion precedes the loss of muscle mass, and is sufficient to induce a decrease in the response to anti-cancer treatments and in the survival of patients.

This cachexia is associated with advanced tumors that present acidosis and metastasis. In this clinical study the investigators would like explore the acid environment effect on the human adipose tissue depletion and more specifically on adipocyte lipolysis.

The main objective of the "TuLip" clinical study is therefore to validate in human subcutaneous and visceral adipocytes that factors secreted by tumor cells cultivated in acid tumor environment stimulate the release of lipids from adipose tissue. Adipocytes retrieves from this study will also be used to validate identified potential lipolytic factors derived from these cells.

Full description

This study is a monocentric clinical study. Patients with BMI < 30 kg/m2 will be recruited in the context of programmed abdominal surgery. In this context, subcutaneous and visceral adipose tissue pieces (1-2 cm3) will be collected to explore the lypolytic response of adipocytes ex-vivo to factors secreted by human cancer cell lines.

Enrollment

5 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Programmed surgeries in the abdominal area in the Department of Surgery and Transplantation at Cliniques Universitaires Saint-Luc under the supervision of Prof. Dr. Benoit Navez.
  • Hospitalization in the context of surgery
  • Caucasian
  • Age between 18 and 60 years (included).
  • Body mass index less than 30 and greater than or equal to 18.5
  • Programmed Nissen fundoplication (to treat hiatal hernia and gastroesophageal reflux) or cholecystectomy (to treat vesicular lithiasis), eventration, or parietal surgery .
  • Adults capable of expressing their wishes.
  • Understanding French

Exclusion criteria

  • Body mass index below 18.5 and above 30.
  • Patients with cancer, infection, autoimmune or inflammatory disease, metabolic syndrome.
  • Patients with beta-blockers, hypoglycemics, anti-diabetics, hypolipidemics.
  • Adults unable to express their will.
  • Not understanding French
  • Patients participating in a clinical trial for a drug treatment.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

Patients with BMI < 30 kg/m2
Experimental group
Description:
Collection of subcutaneous and visceral adipose tissue pieces of 1-2 cm3 during abdominal surgery procedures
Treatment:
Procedure: Nissen Fundoplication, cholecystectomy

Trial contacts and locations

1

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Central trial contact

Camille Lefevre, PhD; Laure Bindels, Professor

Data sourced from clinicaltrials.gov

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