Thoracic Surgery Clinical Trial
— MUSCAOfficial title:
Evaluation of the Prognostic Value of Preoperative Quadriceps and Respiratory Muscle Thickness by Ultrasound Measurement in Cardiac and Thoracic Surgery Patients: a Prospective Observational Study
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 |
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.
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 |
Country | Name | City | State |
---|---|---|---|
France | Chu Dijon Bourgogne | Dijon |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire Dijon |
France,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04865874 -
GDT-PPV Protocol in Thoracic Surgery
|
N/A | |
Active, not recruiting |
NCT02715271 -
Study of TB Lesions Obtained in Therapeutical Surgery
|
||
Completed |
NCT02919267 -
Physiology of Lung Collapse Under One-Lung Ventilation: Underlying Mechanisms
|
N/A | |
Completed |
NCT02964026 -
Study of Clinical Outcomes Associated With the Pulmonary Artery Catheter (PAC) in Cardiac Surgery Patients
|
N/A | |
Recruiting |
NCT03165539 -
Cerebral Oxygen Desaturation and Post-Operative Delirium in Thoracic Surgical Patients
|
||
Terminated |
NCT01320475 -
Epidural Levobupivacaine-sufentanil Versus Epidural Levobupivacaine and Intravenous Ketamine
|
Phase 4 | |
Recruiting |
NCT05045196 -
Health-promoting Family Conversations and Open Heart Surgery
|
N/A | |
Completed |
NCT04507958 -
Electronic Stethoscope Use During Intubation in Full Personal Protective Equipment
|
||
Recruiting |
NCT05060302 -
Prognosis of Right Ventricular Dysfunction Assessed by Speckle Tracking in Postoperative Thoracic Surgery
|
N/A | |
Completed |
NCT05667467 -
The Effect of Care Bundle in Heart Surgery
|
N/A | |
Not yet recruiting |
NCT03275428 -
THRIVE and Non-intubated Thoracic Surgery
|
N/A | |
Not yet recruiting |
NCT05482230 -
Application of Tracheal Intubation in Lateral Position in Thoracic Surgery
|
N/A | |
Enrolling by invitation |
NCT04429009 -
A Randomized Control Trial of ZEPHYRx Gamified Incentive Spirometry Compared to Traditional Spirometry
|
N/A | |
Not yet recruiting |
NCT03628040 -
Erector Spinae Plane Block for Video-assisted Thoracoscopic Surgery
|
Phase 3 | |
Recruiting |
NCT03300622 -
Assessment in Patients After Thoracic Surgery
|
N/A | |
Completed |
NCT00981474 -
Cerebral Autoregulation Monitoring During Cardiac Surgery
|
N/A | |
Completed |
NCT03309280 -
Influence of Different Parameters on Extubation Time After Cardiac Surgery.
|
||
Recruiting |
NCT03820700 -
Using Hypnosis and Virtual Reality During Pre and Postoperative Cardiovascular Surgery.
|
N/A | |
Completed |
NCT03768193 -
Deep Serratus Anterior Plane Block vs Surgically-placed Paravertebral Block for VATS Surgery
|
N/A | |
Recruiting |
NCT04609228 -
Cardiac Surgery Outcomes in Blood-transfusion Acceptors and no Acceptors
|