Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT05684900 |
Other study ID # |
DERINCETRHCELIK001 |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
June 10, 2022 |
Est. completion date |
November 10, 2023 |
Study information
Verified date |
December 2023 |
Source |
Derince Training and Research Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
With the oxygen mask with reservoir, oxygen can be given to patients with FiO2 values that
can reach 80-100%. Reservoir oxygen mask is superior to other oxygen treatment methods with
the high oxygen rate applied.Our hypothesis is that the use of an oxygen mask with a
reservoir will reduce the incidence of respiratory complications in adult patients who will
undergo sedation in the endoscopy unit.
Description:
During the sedation procedure in the endoscopy unit, patients who used a reservoir oxygen
mask will be examined. Patients over the age of 18 and under the age of 70, with ASA 1-2 risk
score, who are planned to be operated under sedation in the endoscopy unit of our hospital
will be included. Patients who do not have verbal and written consent to participate in the
study, have an ASA3-4 risk score, and are scheduled for emergency procedures will be excluded
from the study. No premedication will be applied to patients admitted to the endoscopy unit.
As a standard, intravenous vascular access will be established with a 22 gauge intraket on
the back of the left hand in all patients, 6-10 lt/minute oxygen therapy will be started with
a reservoir mask, and peripheral oxygen saturation, end-tidal CO2, blood pressure arterial
values will be monitored and recorded. These parameters will be monitored and recorded every
five minutes during the procedure. In addition, the sedative agents applied to the patients
and their doses will be recorded. After the procedure, all patients will be taken to the
recovery room, where they will be observed until the modified aldrete score is 9 or higher.
The recovery times of the patients, nausea, vomiting and similar symptoms will be followed
and recorded.