Atelectasis by Lung Ultrasonography in Cesarean Sections

Cesarean Section Clinical Trial

Official title:

Determination of the Effects of General Anesthesia and Spinal Anesthesia Applied in Elective Cesarean Operations on Postoperative Atelectasis by Lung Ultrasonography

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04591327
• Other study ID #: U1111-1258-9377
• Status: Completed
• Start date: August 1, 2020
• Est. completion date: September 16, 2020

Study information

• Verified date: October 2020
• Source: Derince Training and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

In this study aimed to demonstrate that atelectasis developing in the perioperative period of patients undergoing elective cesarean surgery with spinal or general anesthesia methods using lung ultrasound. After Preoperative lung ultrasounds of patients is done, the cesarean operation will be completed with spinal or general anesthesia. In the postoperative period, control lung ultrasounds will be performed and the ultrasound results will be compared in terms of atelectasis in both groups.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 46
• Est. completion date: September 16, 2020
• Est. primary completion date: September 14, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Between 18-40 years

• 37-40 weeks pregnant

• ASA II because of pregnancy

Exclusion Criteria:

• Emergency cesarean sections

• who refuse to participate in the study

• with chronic disease

• Smoker

• with chest deformity

Related Conditions & MeSH terms

• Atelectasis
• Cesarean Section
• Pulmonary Atelectasis

Intervention

Procedure:
• The Effect of General Anesthesia and Spinal Anesthesia on Postoperative Atelectasis by Lung Ultrasonography in Cesarean Sections
Preoperative lung ultrasound will be performed on all patients and baseline values will be recorded. The sensory block level under T10 of the patients who underwent spinal anesthesia in the postoperative period lung ultrasonography will be done after regression. In the postoperative period, lung ultrasonography will be performed in patients undergoing spinal anesthesia when the sensory block level is below T10. In the general anesthesia group, when the neuromuscular block is completely reversed and the Aldrete score is> 9, lung ultrasonography will be performed. The degree of atelectasis will be determined according to the modified LUS score.

Locations

Country	Name	City	State
Turkey	Kocaeli Derince Train and Research Hospital	Kocaeli

Sponsors (1)

Lead Sponsor	Collaborator
Derince Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	incidence of the postoperative atelectasis		two months