Preoperative Highflow Nasal Oxygen Application in Cesarean Under General Anesthesia and Its Effects on Newborn.

K

Kocaeli Derince Education and Research Hospital

Status

Completed

Conditions

Cesarean Delivery Affecting Newborn

Treatments

Device: high flow nasal oxygen device (POİNT)
Device: Face mask

Study type

Interventional

Funder types

Other

Identifiers

NCT03903003
KIA 2018/506

Details and patient eligibility

About

Preoperative Highflow Nasal Oxygen Application in Cesarean Under General Anesthesia and Its Effects on Newborn.

Full description

Patients who will undergo caesarean section under general anesthesia will be included in the study. In the study; preoxygenation is applied to the caesarean sections under general anesthesia in two ways. Group1 includes preoxygenation masked patients.

Enrollment

100 patients

Sex

Female

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • over 18 years old;
  • Patients undergoing elective ceserian operation

Exclusion criteria

  • Patients who refuse to participate in the study;
  • Patients under emergency conditions.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

100 participants in 2 patient groups

preoxygenation mask applied to the cesarean
Active Comparator group
Description:
In order to protect the mother from hypoxia, preoxygenation is performed with face mask before induction of anesthesia.
Treatment:
Device: Face mask
high flow nasal oxygenation applied to the ceserian
Active Comparator group
Description:
In order to protect the mother from hypoxia, preoxygenation is performed with high flow nasal oxygenation mask before induction of anesthesia.
Treatment:
Device: high flow nasal oxygen device (POİNT)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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