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Completed

NCT Number: NCT06268171

Ultrasound Assessment of Rectus Femoris Cross-sectionnal Area Following Lung Transplantation

In France, the profile of patients receiving lung transplants has changed in recent years, mainly due to the advent of treatment for cystic fibrosis. This progress has led to an evolution in the patient profile, with an increase in cases of pulmonary fibrosis or COPD, and an increase in the average age of patients. In these older patients, sarcopenia, a condition characterized by loss of muscle mass, is a major concern, as it exacerbates morbidity and mortality.

After transplantation, patients are at risk of developing neuromyopathy due to their hospitalization in intensive care. There is currently no effective preventive treatment for this condition, underlining the need for early rehabilitation strategies. The combination of sarcopenia and neuromyopathy diminishes their functional capabilities on discharge from the ICU.

Muscle ultrasound, a simple, non-invasive technique, is already used to assess muscle function in intensive care patients. This study aims to evaluate the use of ultrasound to measure muscle loss in lung transplant patients, in particular by examining the rectus femoris muscle. Objectives include observing variations in the surface area of the rectus femoris muscle before and after transplantation, identifying factors influencing this variation, and exploring its relationship with post-transplant morbidity.

In summary, this study seeks to better understand muscle loss in lung transplant patients using ultrasound, in order to identify risk factors and guide the development of post-transplant rehabilitation strategies.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hopital Foch

Suresnes, Hauts de seine, 92151, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patient over the age of 18
  • Patient registered on the lung transplant list at Hôpital Foch for a single or double-lung transplant
  • Patient who did not object to inclusion in the study
  • Patient affiliated to a French health insurance plan

Exclusion criteria

  • Patient listed for a combined transplant (heart-lung, liver-lung, lung-kidney)
  • Patient on national priority list (super-emergency)
  • Pregnant or breast-feeding patient
  • Patient under guardianship

Treatment and study plan

ultrasound measurement of the cross-sectional area of the rectus femoris

Other

ultrasound measurement of the cross-sectional area of the rectus femoris at D-1 and D+3, +7 , +14

Primary outcomes

  1. Evaluation of the change at D7 in the cross-sectional area of the rectus femoris following lung transplantation

    Time frame: Baseline and Day 7

Secondary outcomes

  1. Measure change in cross-sectional area of the rectus femoris at D7 according to LT pattern

    Time frame: Baseline and day 14

  2. Evaluate the relationship between length of stay in intensive care unit and variation in cross-sectional area of the rectus femoris at D7

    Time frame: Baseline and day 7

  3. Determine the relationship between cross-sectional area of the rectus femoris at D-1 and Body Mass Index

    Time frame: Baseline

Sponsors and collaborators

Lead sponsor

Hopital Foch

Other

Registry information

Acronym: EchoSS-TP

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 20, 2024
Registry last updated
Sep 12, 2025

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.

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