Comparison Between the Subglotic Diameter and the Epiphyseal Diameter of the Radius in Children for Prediction of Appropriate Endotracheal Tube Sizes
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03713385 |
|
Recruitment Status : Unknown
Verified March 2019 by Nevert Adel, Mansoura University.
Recruitment status was: Recruiting
First Posted : October 19, 2018
Last Update Posted : March 7, 2019
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Background: In pediatric anesthesia, selection of the appropriate endotracheal tube (ETT) size is an important task because the inappropriate one may lead to much complication. The aim of this study is to compare between the subglotic diameter and the epiphysis diameter of radius measured by ultrasonography for prediction of optimum endotracheal tube size in children.
Methods: Patients aged from 1 to 6 years will be scheduled for elective surgery under general anesthesia and intubation, were enrolled in this study. Patients were randomly divided into three groups according to method of choosing the tube size.
Aged group (n =49): determined the optimal endotracheal tube size according to age of the child (internal diameter [ID] in mm = [age in years + 16] /4) suggested by Cole.4 Subglottic diameter group (n =49): The subglottic transverse diameter was estimated with ultrasonography on the middle of the anterior region of the neck at the level of cricoid cartilage.
Epiphyseal diameter group (n =49): the epiphyseal transverse diameter of the distal radius was estimated with ultrasonography.
Patient descriptive data, size of the selected ETT, number and size of the optimum tube, number of re-intubation due to incorrect size of ETT either smaller or larger were recorded. Subglottic transverse diameter (mm) and time of intubation were measured. After intubation, pulse, respiratory rate, arterial blood saturation, capnograghy and airway pressure were recorded during surgery.
Any airway complications after extubation as edema, stenosis or stridor were also recorded.
| Condition or disease |
|---|
| Prediction of Pediatric Endotracheal Tube Size |
Show detailed description
| Study Type : | Observational |
| Estimated Enrollment : | 147 participants |
| Observational Model: | Case-Control |
| Time Perspective: | Cross-Sectional |
| Official Title: | Comparison Between the Subglotic Diameter and the Epiphyseal Diameter of the Radius in Children for Prediction of Appropriate Endotracheal Tube Sizes |
| Actual Study Start Date : | October 1, 2018 |
| Estimated Primary Completion Date : | July 1, 2019 |
| Estimated Study Completion Date : | August 1, 2019 |
| Group/Cohort |
|---|
|
Aged group (n =49)
Determined the optimal endotracheal tube size according to age of the child (internal diameter [ID] in mm = [age in years + 16] /4) suggested by Cole
|
|
Subglottic diameter group (n =49)
The subglottic transverse diameter was estimated with ultrasonography on the middle of the anterior region of the neck at the level of cricoid cartilage
|
|
Epiphyseal diameter group (n =49)
The epiphyseal transverse diameter of the distal radius was estimated with ultrasonography.
|
- number of the optimum tube size [ Time Frame: 3 months ]number of the optimum tube size used in pediatric patients in each group
- number of re-intubation [ Time Frame: 3 months ]number of re-intubation due to incorrect size of ETT either smaller or larger in each group
- time of intubation [ Time Frame: 3 months ]time was taken for intubation in each group
- airway complications [ Time Frame: 3 months ]airway complications after extubation as edema, stenosis or stridor
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 1 Year to 6 Years (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- Patients aged from 1 to 6 years
- scheduled for elective surgery under general anesthesia and intubation
Exclusion Criteria:
- Patients refusal
- An anticipated difficult airway,
- Any respiratory disease that might cause airway narrowing
- Pre-exiting laryngeal or tracheal pathology
- Any lesion that could cause airway deformity due to fibrosis or the presence of a neck anatomical pathologies that could affect the ultrasound evaluation of the airway
- Any abnormality in the wrist and radius bone
- Any disease after epiphyseal diameter as Rickets or skeletal dysplasia
- Prolonged surgery more than 90 minutes
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03713385
| Contact: Nevert Adel Abdel ghaffar | 01223947977 | neverta@yahoo.com |
| Egypt | |
| Gamal Zakaria | Recruiting |
| Mansourah, Egypt | |
| Contact: Yahya Mohamed Wahba, Ass prof 01211313554 yahyawahba@ymail.com | |
| Sub-Investigator: Yahya Mohamed Wahba, MD | |
| Sub-Investigator: Abdel-Hady El-Gilany, MD | |
| Sub-Investigator: Gamal Zakaria, MD | |
| Responsible Party: | Nevert Adel, lecturer of anesthesia, surgical ICU and pain management, Mansoura University |
| ClinicalTrials.gov Identifier: | NCT03713385 |
| Other Study ID Numbers: |
MansouraU4 |
| First Posted: | October 19, 2018 Key Record Dates |
| Last Update Posted: | March 7, 2019 |
| Last Verified: | March 2019 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

