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Pulmonary Impacts of Anaesthetic Modalities Evaluated by Ultrasound (PULCHO-KNEE)

T

Toulouse University Hospital

Status

Unknown

Conditions

Anesthesia

Treatments

Diagnostic Test: pleuropulmonary ultrasound

Study type

Observational

Funder types

Other

Identifiers

NCT03978169
RC31/18/0379

Details and patient eligibility

About

A prospective, observational, monocentric study aimed at identifying ultrasound changes in anaesthesia on the pulmonary parenchyma after knee arthroplastic surgery using the LUS score in the preoperative, immediate post-operative (D0) and late post-operative (D1) periods.

Full description

Post-operative pulmonary complications are responsible from morbidity and mortality close to cardiovascular complications.

Perioperative and post-operative respiratory changes are secondary to anaesthesia (general anaesthesia, elongated position, tidal volume) and to surgery in particular abdominal and cardiothoracic surgery.

Several risk factors related to patients were identified: age, ASA score> 2, functional dependence, chronic obstructive pulmonary disease, congestive heart failure, obesity, smoking.

Pulmonary ultrasound is a simple and rapid means of monitoring, widely used in resuscitation and developing in anaesthesia.

The hypothesis of the study is that anaesthesia and / or ventilation is responsible for lung lesions observable by ultrasound from the recovery room, even after extra-thoracic surgeries.

To do this, it will perform 3 pleuro-pulmonary ultrasound scans, preoperatively on the day of surgery, post-operatively in the recovery room and the day after surgery. LUS score will be calculated. Preoperative data (morphology, comorbidities), preoperative (ventilation, filling, position, type of anaesthesia - general anaesthesia with intubation or laryngeal mask, spinal anaesthesia- , type of surgery) and postoperative data (constants, oxygen therapy, complications) will be collected.

Enrollment

99 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient undergoing scheduled primary knee arthroplasty :

  • Partial knee replacement surgery

  • Total knee replacement surgery

    • Type of Anaesthesia

  • General anaesthesia with orotracheal intubation

  • General anaesthesia with laryngeal mask

  • Spinal anaesthesia

    • Major Patient
    • Oral non opposition collected after oral information of the study

Exclusion criteria

  • Refusal to participate
  • Preoperative pleural pathology (pleural effusion, pleural symphysis)
  • Pregnancy
  • Patient under authorship or curators
  • non-affiliation to a social security scheme

Trial design

99 participants in 3 patient groups

General anaesthesia with orotracheal intubation
Description:
surgery patients under general anaesthesia with orotracheal intubation
Treatment:
Diagnostic Test: pleuropulmonary ultrasound
General anaesthesia with laryngeal mask
Description:
surgery patient under general anaesthesia with laryngeal mask
Treatment:
Diagnostic Test: pleuropulmonary ultrasound
Spinal anaesthesia
Description:
surgery's patients under Spinal anaesthesia
Treatment:
Diagnostic Test: pleuropulmonary ultrasound

Trial contacts and locations

1

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Central trial contact

LAETITIA BOSCH, MD; Fabrice FERRE, MD

Data sourced from clinicaltrials.gov

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