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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03807375
Other study ID # preoxygenation
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date June 1, 2019

Study information

Verified date January 2019
Source Ankara Diskapi Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study was to evaluate the preoxygenation time by observing patients undergoing preoxygenation with CPAP (Continuous Positive Airway Pressure) and Mask Ventilation in the clinic.


Description:

Criteria for inclusion in the study:

Planned elective bariatric surgery under general anesthesia ASA 1-2 class Between 20-50 years 50 patients

1. Group: Patients undergoing CPAP (Continuous Positive Airway Pressure) during preoxygenation will be included.

2. Group: Patients undergoing preoxygenation without CPAP will be included

In both groups, the time from the anesthesia device to the endtidal O2 90% and the endtidal CO2 value in this order will be recorded.

Heart rate, blood pressure, endtidal O2 and CO2 values will be recorded during preoxygenation and after intubation.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date June 1, 2019
Est. primary completion date May 1, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Inclusion Criteria:

1. Patients between the ages of 20 and 50 years

2. American Society of Anesthesiologists I, II or III

3. Patients with body mass index of 40 and over

Exclusion Criteria:

1. cardiopulmonary disease

2. patients with previous abdominal or thoracic surgery or cerebrovascular disease

3. story of intracranial hypertension or epilepsy

4. patients with a story of difficult tracheal intubation

Study Design


Related Conditions & MeSH terms

  • Time to Reach 90% Endtidal Oxygen During Preoxygenation

Intervention

Other:
CPAP preoxygenation
During preoxygenation, the ventilator device will be placed in spontaneous mode and set as CPAP: 5 cmH2O.

Locations

Country Name City State
Turkey Diskapi Yildirim Beyazit Training Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara Diskapi Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Bouroche G, Bourgain JL. Preoxygenation and general anesthesia: a review. Minerva Anestesiol. 2015 Aug;81(8):910-20. Epub 2015 Jun 5. Review. — View Citation

Nimmagadda U, Salem MR, Crystal GJ. Preoxygenation: Physiologic Basis, Benefits, and Potential Risks. Anesth Analg. 2017 Feb;124(2):507-517. doi: 10.1213/ANE.0000000000001589. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Prevention of desaturation during intubation Prevent desaturation of the apnea period during endotracheal intubation in bariatric surgery 5 minutes
Primary prevention of side effects of hypoxia hypoxia-induced arrhythmia hypotension tachycardia 10 minutes