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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05412095
Other study ID # BERTHOUD 2021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 31, 2022
Est. completion date December 2024

Study information

Verified date February 2024
Source Centre Hospitalier Universitaire Dijon
Contact Vivien BERTHOUD
Phone 0380293528
Email vivien.berthoud@chu-dijon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cardiac and thoracic surgery are major procedures. In order to estimate the operative risk, many scores have been developed, including the Euroscore 2 in cardiac surgery. However, the Euroscore has limitations since it does not assess all the parameters that may influence postoperative complications, such as the patient's general condition or the status of his or her functional reserves. However, it has been shown that the preoperative functional reserves have a significant impact on the patient's risk of developing postoperative complications following major surgery. In addition, there is a strong association between cardiac failure and a well-described decrease in peripheral muscle lean mass (sarcopenia) in patients older than 65 years. Usually, a nutritional assessment is performed during the pre-anesthesia consultation. This assessment is based on clinical and biological criteria that are not totally predictive of the patient's functional reserve status. Lean body mass (muscle) is a well-validated marker for the assessment of patients' functional reserves. However, the techniques used to date are complex and require radiation. This study aims to use ultrasound of muscle groups (respiratory muscles - Quadriceps muscle - Diaphragm) to study the relationship between preoperative muscle mass and postoperative complications in patients over 65 years of age undergoing cardiac or thoracic surgery. This is a prospective observational study to be conducted at the Dijon University Hospital by the cardiovascular anesthesia-intensive care department. A total of 300 patients will participate in this study, and we have planned to complete the project over a 2-year period. The participating patients (if they do not present any exclusion criteria and are not opposed to inclusion) will be included and undergo a muscle ultrasound in the cardiovascular surgery department or the thoracic and pulmonary surgery department the day before their intervention.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 2024
Est. primary completion date July 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Patient 65 years or older - Patients who have not objected to their inclusion in the study - Any patient requiring elective cardiac surgery, with extracorporeal circulation extracorporeal circulation OR - Any patient requiring lung surgery with resection of at least one lobe Exclusion Criteria: - pneumectomy - Person who is not affiliated to national health insurance - Person subject to a measure of legal protection (curatorship, guardianship) - Pregnant, parturient or breastfeeding women - Major unable to express consent - Persons with amputations of the proximal segment of a lower limb - Persons suffering from a pre-existing neuromuscular pathology, tetra or paraplegia - Person who must undergo emergency surgery

Study Design


Intervention

Other:
Ultrasound of the abdominal wall muscles
the measurements will be performed during inspiration and expiration to take into account variability during the respiratory cycle. The examination is performed bilaterally and comparatively and lasts between 3 and 5 minutes.
Ultrasound quadricipital
The examination is performed bilaterally and comparatively and takes between 3 and 5 minutes.
Ultrasound of the diaphragm
The examination is performed bilaterally and comparatively and takes between 5 and 10 minutes.
Ultrasound of the inter-costal muscles
measurements performed bilaterally on a patient in a half-sitting position at 45° and in spontaneous ventilation
Ultrasound of the inter-costal muscles
In spontaneous ventilation, lying down, arms by the side of the body, palms up, head down

Locations

Country Name City State
France Chu Dijon Bourgogne Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Onset of acute renal failure Within 30 days after surgery
Primary Occurrence of a respiratory complication Occurrence of acute respiratory failure in cardiac surgery and occurrence of a severe extra-respiratory complication according to the european perioperative clinical outcome definition in pulmonary surgery Within 30 days after surgery
Primary Occurrence of a cardiovascular complication Within 30 days after surgery
Primary Occurrence of an infectious complication Within 30 days after surgery
Primary Death Within 30 days after surgery
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