The Cricoid Force Necessary to Occlude the Esophageal Entrance: Is There a Gender Difference?

Sponsor
Procare Riaya Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02618863
Collaborator
(none)
60
1
2
3
20.1

Study Details

Study Description

Brief Summary

the investigators have observed that women may require less CF than men to occlude the esophageal entrance, and that the routine use of 30 N in women may actually increase the incidence of airway-related problems. The objective of the current investigation was to test this hypothesis. In this study, real-time visual and dynamic means were used to assess the effectiveness of different forces applied to the cricoid cartilage in occluding the esophageal entrance in men and women. The patency of the esophageal entrance was directly visualized using the Glidescope Video Laryngoscope in anesthetized and paralyzed patients with and without CP. Evidence of closure of the esophageal lumen was confirmed by the inability to introduce a gastric tube (GT) into the esophagus under direct vision. New method , using Cricometer , was used to measure the applied force .

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

Detailed Description

60 (30 men; ages 18 - 50 yr; body mass index < 28 kg/m2 physical status 1, 2 patients were recruited for the study. These patients were to undergo general anesthesia with tracheal intubation. starting force was 20 N in both sex. These forces were standardized by reproducing a new device : cricometer. The sequence of the applied forces was done by using the up and down method in both sex. After preoxygenation, anesthetic induction, muscular relaxation and mask ventilation, the study commenced. Direct laryngoscopy using the Glidescope video laryngoscope was performed and the view of the glottis and the esophageal entrance was video recorded with each CF. 2 attempts to insert a lubricated gastric tube (GT; size 20 F, 12 F) were carried out by a "blinded" operator in each patient. A successful insertion of the GT indicated a patent esophagus. When this occurred while CP was applied, it indicated ineffective CP. An unsuccessful insertion of the GT while CP was applied indicated a non-patent esophagus (effective CP). The position of the esophageal entrance relative to the glottis during CP was assessed from the video recordings.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
The Cricoid Force Necessary to Occlude the Esophageal Entrance: Is There a Gender Difference?
Study Start Date :
Dec 1, 2015
Anticipated Primary Completion Date :
Feb 1, 2016
Anticipated Study Completion Date :
Mar 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 1 , cricoid pressure

30 male

Device: Cricoid pressure
Applying cricoid pressure and testing its effectiveness using gastric tube . in addition , by using the cricometer , the CP 50 is defined and compared in both gender

Active Comparator: 2,cricoid pressure

30 female

Device: Cricoid pressure
Applying cricoid pressure and testing its effectiveness using gastric tube . in addition , by using the cricometer , the CP 50 is defined and compared in both gender

Outcome Measures

Primary Outcome Measures

  1. Necessary force of CP to occlude the esophagus in female versus male . an up and down method will define the CP 50 in each gender . A comparison between CP50 in both sex will define exactly our outcome : Is there a gender difference . [24 hours]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • ASA 1 - 2

  • Easy Identification cricoid cartilage

  • No contre indication to CP

Exclusion Criteria:
  • obese patients

  • ASA2 & ASA3

  • contre indication to CP

Contacts and Locations

Locations

Site City State Country Postal Code
1 Procare Riaya Hospital Al Khobar Estern Saudi Arabia 31952

Sponsors and Collaborators

  • Procare Riaya Hospital

Investigators

  • Study Director: kamal abdulkhaleq, MD, Procare Riaya Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahed ZEIDAN, Dr.AHED ZEIDAN, Procare Riaya Hospital
ClinicalTrials.gov Identifier:
NCT02618863
Other Study ID Numbers:
  • PRH7
First Posted:
Dec 2, 2015
Last Update Posted:
Feb 17, 2016
Last Verified:
Feb 1, 2016

Study Results

No Results Posted as of Feb 17, 2016