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Clinical Trials/NCT04116567
NCT04116567
Completed
Not Applicable

Lung Ultrasonography for the Assessment of Perioperative Atelectasis After Laparoscopic Gynecologic Oncologic Surgery

SONNINO CHIARA1 site in 1 country80 target enrollmentOctober 3, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pulmonary Atelectasis
Sponsor
SONNINO CHIARA
Enrollment
80
Locations
1
Primary Endpoint
Assess if LUS score measured after surgery is higher that LUS score measured before induction of anesthesia
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study evaluates the influence of surgical and anesthesia-related variable on atelectasis formation during laparoscopic gynecologic oncologic surgery by lung ultrasound.

Detailed Description

Approximately 50% of patients undergoing general anesthesia are hypoxemic. Anaesthesia, paralysis, high concentrations of oxygen, inadequate level of PEEP, capnoperitoneum, Trendelenburg position all result in persistent atelectasis. Lung ultrasound is a safe and accurate bedside tool useful to study lung aeration. The aim of the investigator's study was to assess the impact of general anesthesia and laparoscopic gynecologic oncologic surgery on post-operative atelectasis and related oxygenation changes using lung ultrasound.

Registry
clinicaltrials.gov
Start Date
October 3, 2018
End Date
June 28, 2019
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
SONNINO CHIARA
Responsible Party
Sponsor Investigator
Principal Investigator

SONNINO CHIARA

Registered Anesthesiologist

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Eligibility Criteria

Inclusion Criteria

  • Patients older than 18 yo undergoing laparoscopic surgery for gynecologic surgery who provide written informed consent.

Exclusion Criteria

  • age \< 18 yo;
  • pregnancy;
  • refused to partecipate;
  • known pulmonary metastasis;
  • preexisting pulmonary conditions (COPD, pleural effusion, pulmonary consolidations, lung edema, pulmonary embolism);
  • anesthesia with mechanical ventilation in the 2 weeks.

Outcomes

Primary Outcomes

Assess if LUS score measured after surgery is higher that LUS score measured before induction of anesthesia

Time Frame: The outcome will be measured 10 minutes after extubation

Each lung will be divided in 6 areas and a score from 0 to 3 will be assigned to each field depending on the loss of aereation detected by ultrasound. LUS score will range between 0 and 36. Lung ultrasound will be performed before induction of anesthesia and 10 minutes after extubation.

Correlation between the increase of LUS score after surgery and surgical or anesthesia-related variables.

Time Frame: The outcome will be measured 10 minutes after extubation

Logistic regression will be applied to consider the correlation between Delta LUS and the following variables: * lenght of surgery * duration of pneumoperitoneum * angle of Trendelenburg potision * duration of mechanical ventilation * intraoperative fluids * duration of apnea from induction to intubation

Study Sites (1)

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