Skip to content

Comparison of Two Mechanical Ventilation Modes on Oxygenisation

Comparison of Two Mechanical Ventilation Strategies on Tissue Oxygenization of Patients Undergoing Bariatric Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04389047
Enrollment
30
Registered
2020-05-15
Start date
2012-01-10
Completion date
2018-03-30
Last updated
2020-05-15

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

Conditions

Bariatric Surgery Candidate, Hypoxia, Mechanical Ventilation, Tissue Damage

Keywords

bariatric surgery, tissue oxygenization, ventilation

Brief summary

Comparison the effect of two different mechanical ventilation modes on tissue oxygenization.

Detailed description

Aim of the study is to evaluate and compare the effects of two different mechanical ventilation modes as Volume Controlled Mechanical Ventilation (VCV) and Pressure Controlled Mechanical Ventilation (PCV) on non invasive tissue oxygenization levels of patients who scheduled for bariatric surgery.

Interventions

None listed

Sponsors

Bagcilar Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Patients with Body Mass Index 35 - 50 kg/m2 Patients classified as American Society of Anesthesiologist (ASA) 1-2-3 classification Patients elected for Bariatric surgery

Exclusion criteria

Patients who wants to reject of study participation Patients who has any surgical complication during the surgery period Patients with decompensated cardiac failure Patients with Moderate or Severe obstructive/restrictive lung disease Patients with Reynaud disease Patients with Buerger phenomena Patients whıo has Intraoperative airway pressure more than 45 cmH2O Patients who had previous thoracic surgery Patients with Negative Modified Allen test

Design outcomes

Primary

MeasureTime frameDescription
Peripheral oxygen saturation-2post operative 1.hour - 4. hour - 8. hour - 12. hour - 24.hourPeripheral Oxygen Saturation (SpO2)
Arterial blood gas analysisPeroperative 0. minute - 30. minute - 60. minuteLactate, Ph, Arterial oxygen pressure, Arterial Carbondioxide pressure, Oxygen Saturation
Arterial blood gas analysis-2post operative 1.hour - 4. hour - 8. hour - 12. hour - 24.hourLactate, Ph, Arterial oxygen pressure, Arterial Carbondioxide pressure, Oxygen Saturation
Peripheral oxygen saturationperoperative 0. minute - 15. minute - 30. minute - 45. minute - 60. minutePeripheral Oxygen Saturation (SpO2)
Oxygenizationperoperative 0. minute - 15. minute - 30. minute - 45. minute - 60. minutePeroperative Non invazive technique of Superficial Tissue Oxygenization
Oxygenization-2post operative 1. hour - 4. hour - 8. hour - 12. hour - 24.hourPost operative Non invazive technique of Superficial Tissue Oxygenization

Secondary

MeasureTime frameDescription
Postoperative hemodynamic measurementspost operative 1.hour - 4. hour - 8. hour - 12. hour - 24.hourHeart rate, Mean Arterial Blood Pressure
Carbondioxideperoperative 15. minute - 30. minute - 45. minute - 60. minuteEnd tidal Carbondioxide measurement
Peroperative hemodynamic measurementsperoperative 0. minute - 15. minute - 30. minute - 45. minute - 60. minuteHeart rate, Mean Arterial Blood Pressure

Outcome results

None listed

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