Skip to main content
OpenTrials
Terminated

NCT Number: NCT05417581

Mitochondrial Oxygraphy on Subcutaneous and Peri-visceral Adipose Tissue: Influence of Body Composition

The objective of this study is to adapt the oxygraphy technique on human adipocytes and to characterize respiration measurements according to patients' body mass index and white adipose tissue localization (subcutaneous vs visceral).

Why the study stopped: Difficulty of recruitment for Groups 1 and 3 not allowing all recruitment to be carried out over a reasonable period of time, it was decided to close this project
Terminated

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU clermont-ferrand

Clermont-Ferrand, France

About this study

During digestive surgery: oncological and bariatric surgery, it is possible to collect a small volume of subcutaneous and epiplonic adipose tissue (10-20 cc). We wish to collect these samples in order to develop the technique of oxygenography on permeabilized adipocytes. In order to characterize these measurements, they will be related to the clinical data of the patients usually collected in the framework of the preoperative assessment including the body mass index (BMI). The measured adipocyte data will thus be normalized to three BMI classes: ≤ 20, > to 20 < 30, and ≥ to 30 kg∙m-2.

Primary end point is to validate the measurement of mitochondrial respiration under oxidophosphorylating conditions by determining indicators of the distribution of mitochondrial respiration values (mean, standard deviation, skewness, kurtosis, coefficient of variation) as a function of patients' body mass index.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients undergoing oncological, bariatric, parietal surgery
  • Patients able to give an informed consent
  • Patients affiliated to an Health Care insurance
  • Patients aged over 18

Exclusion criteria

  • Patients under guardianship, curatorship or deprived of freedom
  • Pregnant or breastfeeding women
  • Participation refusal
  • Patients under chemotherapy
  • Patients with peritonitis and infectious parietal processes

Treatment and study plan

adipose surgery

Procedure

A quantity of adipose tissue equivalent to 10-20 cubic centimeter will be removed subcutaneously and from the omentum during surgical procedures (oncological, bariatric)

Primary outcomes

  1. Evaluation of mitochondrial respiration on adipose tissue by oxygraphy

    Time frame: day 1

    Mitochondrial respiration measurements in oxydophosphorylated conditions. For each patient measurements using ADP and carbohydrate or lipid substrates of the respiratory chain complexes for both the subcutaneous and the visceral tissue.

Secondary outcomes

  1. mitochondrial respiration values depending on patients BMI by oxygraphy

    Time frame: day 1

    Identification of mitochondrial respiration discrimination factors

  2. comparing mitochondrial respiration values depending on tissue location by oxygraphy

    Time frame: day 1

    Identification of mitochondrial respiration discrimination factors

  3. comparing mitochondrial respiration values depending on anthropometric data by oxygraphy

    Time frame: day 1

    Identification of mitochondrial respiration discrimination factors

Sponsors and collaborators

Lead sponsor

University Hospital, Clermont-Ferrand

Other

Registry information

Acronym: OxMiTiAd

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jun 14, 2022
Registry last updated
Aug 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.