The Benefit of Preparation in Respiratory Physiotherapy Before a Sternotomy in the Context of Cardiac Surgery

NCT ID: NCT06153550

Last Updated: 2023-12-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-09-01

Study Completion Date

2021-11-10

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Sternotomy

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Cardiac surgery Sternotomy respiration Spirometry pulse oximetry

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Patients who have sternotomy

Patients who have sternotomy wll be included. They will have preparation in Respiratory Physiotherapy before sternotomy.

preparation in Respiratory Physiotherapy

Intervention Type OTHER

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.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

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.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Centre Hospitalier Universitaire de Saint Etienne

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Andranik PETROSYAN, MD

Role: PRINCIPAL_INVESTIGATOR

CHU SAINT-ETIENNE

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

CHU Saint-Etienne

Saint-Etienne, , France

Site Status

Countries

Review the countries where the study has at least one active or historical site.

France

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

IRBN522021/CHUSTE

Identifier Type: -

Identifier Source: org_study_id