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Comparison of Volume Controlled Ventilation and Pressure Controlled Ventilation in Laparoscopic Bariatric Surgery

Comparison of Volume Controlled Ventilation and Pressure Controlled Ventilation in Terms of Respiratory Mechanics in Laparoscopic Bariatric Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03758937
Enrollment
62
Registered
2018-11-29
Start date
2016-04-01
Completion date
2017-08-01
Last updated
2018-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bariatric Surgery

Keywords

bariatric surgery, volume-controlled ventilation, pressure-controlled ventilation

Brief summary

The purpose of this study is to compare volume controlled-ventilation (VCV) and pressure-controlled ventilation (PCV) in terms of pulmonary gas exchange, respiratory mechanics and arterial blood gas values in patients undergoing laparoscopic bariatric surgery.

Detailed description

Today, morbid obesity has become a global problem. It is not clear which mechanical ventilation mode will be used in bariatric surgery, which is one of the treatment options of these patients. VCV is the most commonly used mode to ventilate anesthetized patients. However, especially in obese patients, high airway pressures and hypoxia may occur due to increased intrapulmonary shunts. Therefore, we aimed to investigate the potential of PCV strategy to improve pulmonary gas exchange, respiratory mechanics and arterial blood gas values according to VCV in patients undergoing bariatric surgery.

Interventions

Sponsors

Antalya Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years or above, * ASA II patients * BMI \> 40 kg / m2 * No serious comorbidity.

Exclusion criteria

* Unstable patients during the operation * The requirement for mechanical ventilation in the postoperative period.

Design outcomes

Primary

MeasureTime frameDescription
Partial oxygen pressure5 minutes after inductionAssessed 5 minutes after induction by using arterial blood gas analysis.

Secondary

MeasureTime frameDescription
Partial carbon dioxide pressure - end-tidal carbon dioxide pressure5 minutes after induction, 30 minutes after pneumoperitoneum, through surgery completion, an average of 90 minutesAssessed 5 minutes after induction, 30 minutes after pneumoperitoneum and through surgery completion, an average of 90 minutes by using arterial blood gas analysis and end-tidal monitor.
Peak airway pressure5 minutes after induction, 30 minutes after pneumoperitoneum, through surgery completion, an average of 90 minutesAssessed 5 minutes after induction, 30 minutes after pneumoperitoneum and through surgery completion, an average of 90 minutes by using the patient monitor.
Partial carbon dioxide pressure5 minutes after induction, 30 minutes after pneumoperitoneum, through surgery completion, an average of 90 minutesAssessed 5 minutes after induction, 30 minutes after pneumoperitoneum and through surgery completion, an average of 90 minutes by using arterial blood gas analysis.
Inspired oxygen pressure / Fractional oxygen ratio5 minutes after induction, 30 minutes after pneumoperitoneum, through surgery completion, an average of 90 minutesAssessed 5 minutes after induction, 30 minutes after pneumoperitoneum and through surgery completion, an average of 90 minutes
Alveolar-arterial oxygen gradient pressure5 minutes after induction, 30 minutes after pneumoperitoneum, through surgery completion, an average of 90 minutesAssessed 5 minutes after induction, 30 minutes after pneumoperitoneum and through surgery completion, an average of 90 minutes by using formula (D(A-a) O2).
Dynamic compliance5 minutes after induction, 30 minutes after pneumoperitoneum, through surgery completion, an average of 90 minutesAssessed 5 minutes after induction, 30 minutes after pneumoperitoneum and through surgery completion, an average of 90 minutes by using formula (Tidal volume/peak airway pressure - Positive end-expiratory pressure)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026