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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06153550
Other study ID # IRBN522021/CHUSTE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2021
Est. completion date November 10, 2021

Study information

Verified date November 2023
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The sternotomy has some influence on the respiratory system after cardiac surgery, considerably increasing the risk of perioperative and postoperative breathing. There is respiratory preparation before cardiac surgery using local physiotherapeutic guidelines.


Description:

The aim of the study is to have a quantification of this preparation spirometry: before starting the preparation and at the end of the preparation (right before surgery) by comparing the spirometric and pulse oximetry information. The prospective study will be conducted on 25 patients, who will be selected consecutively without randomization.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date November 10, 2021
Est. primary completion date November 10, 2021
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Patient with indication of cardiac surgery Exclusion Criteria: - Patient with a Body Mass Index (BMI) > 30 - Restrictive patient - Obstructive patient - Asthmatic - Chronic Obstructive Pulmonary Disease (COPD) - History of pulmonary fibrosis, tuberculosis - Coronary patients with stenosis of the common trunk. - Emergency and lifesaving surgeries - History of thoracic trauma - Severe kyphotic patients - History of radiotherapy - Patients with neuromuscular disease - Patients with thoracic cage involvement (pectus excavatum, post thoracic surgery) - Patients with emphysema - Patients with dilated bronchi

Study Design


Related Conditions & MeSH terms


Intervention

Other:
preparation in Respiratory Physiotherapy
preparation in Respiratory Physiotherapy consist to: 3 sessions per week with the physiotherapist spirometry and pulse oximetry test 3 weeks before surgery, the day before surgery and the day after surgery.

Locations

Country Name City State
France CHU Saint-Etienne Saint-Étienne

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analysis of the evolution of the pulmonary function by Forced spirometry. Measured by spirometry and pulse oximetry results. 3 weeks before, the day before and the day after surgery.
Secondary Analysis of the evolution of the pulmonary function by Resistance Measured by spirometry and pulse oximetry results. 3 weeks before, the day before and the day after surgery.
Secondary Analysis of the evolution of the pulmonary function by Lung volumes Measured by spirometry and pulse oximetry results. 3 weeks before, the day before and the day after surgery.
Secondary Analysis of the evolution of the pulmonary function by Dissemination capacity, Measured by spirometry and pulse oximetry results. 3 weeks before, the day before and the day after surgery.
Secondary Analysis of the evolution of the pulmonary function by Flow / volume curves Measured by spirometry and pulse oximetry results. 3 weeks before, the day before and the day after surgery.
Secondary Analysis of the evolution of the pulmonary function by Peripheral saturation Measured by spirometry and pulse oximetry results. 3 weeks before, the day before and the day after surgery.
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