Impact of Change of Head and Neck Position on Cricothyroid Membrane Localization and Membrane Height in Parturient Patients

Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04138121
Collaborator
(none)
50
1
1
1.5
33.1

Study Details

Study Description

Brief Summary

The cricothyroid membrane acts a route through which the upper airway can be accessed in order to provide oxygen and ventilation to patients. The need to provide oxygen and ventilation to patients is essential particularly under general anesthesia, where patients may lose the ability to breathe for themselves. Access through this membrane to provide oxygen and ventilation is critical in emergency situations where other traditional means to access the airway (e.g through endotracheal ventilation, supraglottic airway devices or face mask ventilation) have failed. It is known that due to the physiological changes of pregnancy, the upper airway of the body undergoes changes that can make accessing the airway through traditional means more difficult. Ultrasound is becoming increasingly popular due to its ability to identify the cricothyroid membrane, to improve success in accessing the airway through the cricothyroid membrane. Studies to date in non pregnant adults have shown that alterations in the head and neck position can alter the position and size of the cricothyroid membrane. No study to date however has looked at how changing the position of the head and neck effects the position and size of the cricothyroid membrane in pregnant patients. It is important to study these changes in the pregnant population, given the physiological changes of pregnancy that make accessing the airway through traditional methods more difficult in non pregnant patients. The investigators hypothesize that in pregnant patients in the third trimester, that changing the head from the neutral to maximally extended neck position will alter the position of the cricothyroid membrane in relation to anatomical skin markings between positions. The investigators also hypothesize that in pregnant patients in the third trimester that changing the head from the neutral to maximally extended neck position will increase the size of the cricothyroid membrane. The investigatorsalso aim to determine at what position in the neck a theoretical standardized incision will allow access to the cricothyroid membrane.

Condition or Disease Intervention/Treatment Phase
  • Device: Ultrasound
N/A

Detailed Description

This is an observational study.

Participants:
  1. One of two anesthesiologists trained in cricothyroid membrane ultrasound scanning technique in pregnant population (study investigators)

  2. Subjects to be assessed: pregnant patients in their third trimester on the labor and delivery floor comfortable enough to take part in the study

Two anesthesiologists will undergo ultrasound imaging training by an expert staff anesthesiologist whom is already trained in the procedure. As per previous published evidence on this, the investigator will need to correctly identify the location of cricothyroid membrane and its height in 15 volunteers. This will constitute the standardized training component of the study.

Upon admission to the Labor and Delivery floor, women will be further explained the protocol and asked to sign the consent form. Then, they will have the cricothyroid membrane assessed, as per description above, and quantitative assessment will be performed. Firstly, quantitative assessment of the height of the cricothyroid membrane will be performed in the supine position (with left uterine displacement) with the neck in the neutral position. The central point of the cricothyroid membrane will be marked using a removable skin ink marker. The patient will then be asked to fully their neck. The change in distance of the midpoint of the cricothyroid membrane from the neutral head and neck position to fully extended positioned will be performed, as will the change in height of the cricothyroid membrane between the two positions.

Quantitative assessment for change in central cricothyroid membrane distance will be done with measuring central points marked on the patients neck with skin marker ink. Quantitative assessment of change in cricoid thyroid membrane will be conducted using caliper measuring software build into the ultrasound machinery. Finally, the investigators will establish the starting distance above the sternal notch over which a theoretical 8cm incision in the neck which will overlie the cricothyroid membrane. This will be done by measuring the distance above the sternal notch with a surgical measuring ruler.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Impact of Change of Head and Neck Position on Cricothyroid Membrane Localization and Membrane Height in Parturient Patients: an Observational Study
Actual Study Start Date :
Nov 4, 2019
Actual Primary Completion Date :
Dec 20, 2019
Actual Study Completion Date :
Dec 20, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Ultrasound

Ultrasound measurements of the cricothyroid membrane.

Device: Ultrasound
Ultrasound scan of the cricothyroid membrane

Outcome Measures

Primary Outcome Measures

  1. Cricothyroid membrane position change [30 minutes]

    To measure the distance the center of the cricothyroid membrane changes position on ultrasound between neutral and maximal neck extension in third trimester patients.

Secondary Outcome Measures

  1. Cricothyroid membrane size change [30 minutes]

    To measure the distance that the size of the cricothyroid membrane changes position on ultrasound between neutral and maximal neck extension in third trimester patients.

  2. Distance above sternal notch [30 minutes]

    The starting distance above the sternal notch in the neck over which an 8cm incision in the neck should overlie the cricothyroid membrane

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant patients in third trimester (>28/40 weeks)

  • Ability to understand the rationale of the study assessments and to provide signed consent.

Exclusion Criteria:
  • Neck arthritis

  • Cervical stenosis

  • Known cervical degenerative disc disease

  • Rheumatoid Arthritis

  • Any restriction of neck movement

  • Upper limb neurology

  • Patient refusal

  • Non pregnant patients

  • Pregnant patients less than 28 weeks pregnant

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mount Sinai Hospital Toronto Ontario Canada M5G1X5

Sponsors and Collaborators

  • Samuel Lunenfeld Research Institute, Mount Sinai Hospital

Investigators

  • Principal Investigator: Naveed Siddiqui, MD, MOUNT SINAI HOSPITAL

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
ClinicalTrials.gov Identifier:
NCT04138121
Other Study ID Numbers:
  • 19-05
First Posted:
Oct 24, 2019
Last Update Posted:
Sep 11, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Samuel Lunenfeld Research Institute, Mount Sinai Hospital

Study Results

No Results Posted as of Sep 11, 2020