Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04991727
Other study ID # KYLL-2021-277
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 21, 2021
Est. completion date December 23, 2023

Study information

Verified date July 2021
Source General Hospital of Ningxia Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Peri - operative ultrasonography was used to evaluate the effects of protective lung ventilation on the postoperative lungs of obese patients.The purpose of this study was to apply ultrasound lung ventilation area score to the monitoring of pulmonary complications in patients with postoperative obesity.To verify the reliability and practicability of perioperative lung ultrasound quantitative scoring.


Description:

Ultrasound lung ventilation area score was applied to monitor the pulmonary complications of patients after obesity operation to verify the perioperative period. The reliability and practicability of quantitative lung ultrasound score to clarify the effect of protective lung ventilation under perioperative pulmonary ultrasound monitoring on obesity patients.To guide the management of mechanical ventilation under general anesthesia and the prevention and treatment of postoperative pulmonary complications


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 23, 2023
Est. primary completion date October 23, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - enrollment of patients aged 18 years or above; - Eligible adult patients had an American Society of Anesthesiologists (ASA) physical status classification of I to IV - undergoing elective or expedited nonurgent, noncardiac surgery with general anesthesia Exclusion Criteria: - patient refusal; - morbid obesity (BMI >40 kg/ m²); - American Society of Anesthesiologists (ASA) physical status categories IV-V; - previous intrathoracic procedure; - severechronic obstructive pulmonary disease (forced expiratory volume in 1 s <30% of the predicted value; - a contraindication to radial artery cannulation.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
recruitment maneuvers
Immediately after endotracheal intubation is completed First RM (pulmonary retraction), maintain pressure at 40cmH2O for 30s, and then Mechanical ventilation was maintained with 7cmH2O PEEP, and the RMS was repeated every 30 minutes until the end of surgery

Locations

Country Name City State
China General Hospital of Ningxia Medical University Yinchuan Ningxia

Sponsors (1)

Lead Sponsor Collaborator
General Hospital of Ningxia Medical University

Country where clinical trial is conducted

China, 

References & Publications (2)

Costamagna A, Pivetta E, Goffi A, Steinberg I, Arina P, Mazzeo AT, Del Sorbo L, Veglia S, Davini O, Brazzi L, Ranieri VM, Fanelli V. Clinical performance of lung ultrasound in predicting ARDS morphology. Ann Intensive Care. 2021 Mar 29;11(1):51. doi: 10.1186/s13613-021-00837-1. — View Citation

Wangüemert Pérez AL. Clinical applications of pulmonary ultrasound. Med Clin (Barc). 2020 Apr 10;154(7):260-268. doi: 10.1016/j.medcli.2019.11.001. Epub 2020 Jan 8. Review. English, Spanish. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Lung ultrasound scoring Four signs were used in lung ultrasound scoring
Lung ultrasound score: N (0): pleural line and A line, less than 3 B lines; B1 (1 mark): More than 3
B line; B2 (2 points): Fuse line B; C (3 points): Signs of lung consolidation. The higher the score is, the worse the pulmonary ventilation status is.
When scoring, the sign with the greatest severity is taken as the score value of the examination area. There are 12 examination areas in both lungs, so we have a LUS
The score is between 0 and 36
in the morning of the first day
Secondary Results of arterial blood gas analysis PCO2 entering the operating room, in the morning of the first day ,the second day , the third day after surgery
Secondary Mechanical ventilation parameter peak inspiratory pressure entering the operating room, in the morning of the first day ,the second day , the third day after surgery
See also
  Status Clinical Trial Phase
Completed NCT06148701 - Preoperative Anesthesia Automatic System:a Retrospective Cohort Study
Completed NCT04000490 - External Validation of the SCARE Score
Recruiting NCT03466905 - Does Assessment of Ambulance Medical Service Leads to Reduced Number of Transports to the Emergency Room? N/A
Completed NCT03233789 - Development and Validation of an ADL-score Based on FIM and EBI
Completed NCT04706351 - Arabic Version of Identification of Functional Ankle Instability Questionnaire
Completed NCT04389255 - Developing a Balance Assessment System
Recruiting NCT05789472 - The Relationship Between Reaction Time and Executive Functions in Female Athletes N/A
Completed NCT05896085 - Game Based Assessment of Emotion-regulation Skills in College Students N/A
Completed NCT05966779 - Physical Therapy in Lipedema Surgery
Not yet recruiting NCT04889456 - Standardizing Right Hemicolectomy for Colon Cancer N/A
Completed NCT03999866 - Preoperative Assessment of Difficult Laryngoscopy Using Different Videolaryngoscopes N/A
Recruiting NCT04073836 - GMA and Peri in Moderate-late Preterms
Completed NCT05285150 - The Weighting of the Balance
Completed NCT04784819 - Turkish Version of Occupational Balance-Questionnaire (OB-Quest)