Study Examining Parker-Flex Endotracheal Tube for Obese Patients

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Baylor College of Medicine

Status

Completed

Conditions

Obesity

Treatments

Device: Parker Flex-Tip® tracheal tube
Device: Portex® Tracheal Tube

Study type

Interventional

Funder types

Other

Identifiers

NCT01894178
H-31550

Details and patient eligibility

About

A recent article examined the use of Parker Flex-Tip tubes to standard ETTs for oral fiberoptic intubation and concluded that there was a significant benefit in terms of difficulty encountered when using the Parker Flex-Tip. The Parker Flex-Tip tracheal tube has a flexible, curved, and tapered tip design different from traditional endotracheal tubes. The design allows the tube to lie closely against the fiberoptic scope that is often used to facilitate intubation, resulting in a smaller gap between the ETT and the fiberoptic scope. This may allow the ETT to clear anatomic obstructions more easily. The patients they examined had an average body mass index (BMI) categorized as normal weight. To our knowledge, there have not been any studies that have investigated the use of the Parker Flex-Tube for fiberoptic intubations in patients categorized as obese by BMI. Our hypothesis is that the Parker Flex-Tip ETT results in easier passage of the ETT over a fiberoptic scope during elective fiberoptic intubation of obese patients in comparison to a traditional ETT.

Full description

This is a randomized, double-blinded study. Neither the patient nor the anesthesia practitioner advancing the ETT will know the group to which the patient has been assigned. On the day of surgery, participants will be randomized 1:1 to one of two groups. Both groups will be electively intubated with a fiberoptic scope. One group will be intubated using a Parker-Flex endotracheal tube and the second group of will be intubated with a standard endotracheal tube. There will be an equal probability of being assigned to either group. No placebo or control group will be used. Randomization will be computer-generated and assignments will be enclosed in sealed envelopes to provide allocation concealment. The anesthesiology technician involved in the case will open the envelope at the start of the case and will not be blinded to the study, due to the fact that the technician must prepare the endotracheal tube for the fiberoptic intubation.

Enrollment

60 patients

Sex

All

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • BMI of 30 or greater
  • American Society of Anesthesiologists (ASA) Physical Status Classification I- III
  • Patients scheduled for elective procedures requiring general anesthesia and endotracheal intubation.

Exclusion criteria

  • Predicted difficult airway based on physical exam and patient's history
  • Rapid sequence intubation indicated (patients who require to be intubated as quickly as possible)
  • Prior trauma or surgery in the oropharynx/larynx
  • Known abnormal laryngeal structures (tumors)
  • Infectious and toxic conditions
  • Cervical spine instability
  • Emergency surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups

Parker Flex-Tip® Tracheal Tube
Active Comparator group
Description:
Intubation of obese patients with the Parker Flex-Tip® Tracheal Tube
Treatment:
Device: Parker Flex-Tip® tracheal tube
Portex® Tracheal Tube
Active Comparator group
Description:
Intubation of obese patients with the Portex® Tracheal Tube
Treatment:
Device: Portex® Tracheal Tube

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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