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NCT04259918 Clinical Trial

Effect of Alveolar Recruitment Maneuver on Postoperative Pain

Pain, Postoperative Clinical Trial

Official title:
Effect of Alveolar Recruitment Maneuver on Postoperative Pain After Bariatric Surgery

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04259918
Other study ID # Gil2019-1
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 25, 2020
Est. completion date December 31, 2020

Study information
Verified date February 2020
Source Gachon University Gil Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Control group: no additional procedure Low ARM group : recruitment maneuver of 30cmH2O High ARM group: recruitment maneuver of 60cmH2O

Description:

After random assignment of group, Control group: no additional procedure apply, Low ARM group : after surgical trocha out after bariatric surgery, applying 30cmH2O recruitment maneuver 5 times every 5 seconds, High ARM group: after surgical trocha out after bariatric surgery, applying 60cmH2O recruitment maneuver 5 times every 5 seconds

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 90
Est. completion date December 31, 2020
Est. primary completion date November 30, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients who scheduled for elective bariatric surgery

Exclusion Criteria:

- uncontrolled cardio-vascular disease, active pulmonary disorder

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Alveolar recruitment maneuver
Applying 30 or 60 cmH2O of alveolar recruitment maneuver 5 times every 5 min at the end of bariatric surgery

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Gachon University Gil Medical Center

Outcome
Type Measure Description Time frame Safety issue
Primary numeric rating scale for postoperative pain score (0 no pain-10 severe pain) up to postoperative 24 hour
Primary Quality of recovery (QoR40) for Postoperative comfort score 40 (extremely poor quality of recovery) to 200 (excellent quality of recovery) up to postoperative 24 hour
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