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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02620540
Other study ID # KEK-ZH-Nr. 2015-0191 - Part 2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 2015
Est. completion date November 2017

Study information

Verified date May 2018
Source University Children's Hospital, Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this prospective single center study is to investigate if a developed algorithm is more accurate than the Broselow Tape (BT). For this study 500 patients are required to collect anonymized data (length, weight, age, anaesthesia material used during anaesthesia) for achieving a power of 80% during statistical analysis. The main hypothesis ist that the algorithm has a better accuracy than the BT.


Description:

This prospective single center study is performed at the university children's hospital zurich. Patients planned for surgery in general anaesthesia with intubation, aged 0 to 16 years and with a body length suitable for the emergency tapes can be included in this study. Patient and parental information is performed during the pre-anaesthetic visit.

After written consent the patient will be included. Patient ́s length and weight will be measures earliest one day before data collection. Data collection during anaesthesia has no influence on the daily anaesthesia routine and has no impact on patient safety and anaesthesia. Patient's data is made anonymous for further inspection. Data is documented in Microsoft Excel and statistical analysis calculated with SPSS.

500 patients are needed for a power of 80%. Primary outcome parameter is length- based weight estimation, secondary outcome parameters are length-based age estimation and the correctness of recommended anaesthesia material (endotracheal tube, laryngeal mask, oropharyngeal mask and face mask). Both tools (algorithm and BT) will be compared with each other regarding primary and secondary outcome parameters.


Recruitment information / eligibility

Status Completed
Enrollment 312
Est. completion date November 2017
Est. primary completion date February 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 16 Years
Eligibility Inclusion Criteria:

- body length suitable with the investigated emergency tapes

- all patients aged 0 -16 years

- receiving general anaesthesia with intubation or laryngeal mask

Exclusion Criteria:

- Already included in this study once

- missing patient or parental consent

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Accuracy of an algorithm and the Broselow Tape
Computer based comparison of the two devices based on collected patient data

Locations

Country Name City State
Switzerland University Childrens Hospital Zurich

Sponsors (1)

Lead Sponsor Collaborator
University Children's Hospital, Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary length-based weight-estimation by algorithm The by the algorithm estimated bodyweight based on the patient's Body length is investigated regarding the estimations accuracy and cases in the +/- 10% interval during anaesthesia
Secondary length based age estimation The by the algorithm estimated age based on the patient's body length is investigated regarding the estimations accuracy during anaesthesia
Secondary size of endotracheal tube The by the algorithm suggested endotracheal tube based on the patient's Body length is investigated regarding the correctness during anaesthesia
Secondary size of laryngeal mask The by the algorithm suggested laryngeal mask based on the patient's Body length is investigated regarding the correctness during anaesthesia
Secondary size of facemask The by the algorithm suggested facemask based on the patient's body length is investigated regarding the correctness during anaesthesia
Secondary size of oropharyngeal tube The by the algorithm suggested oropharyngeal tube based on the patient's Body length is investigated regarding the correctness during anaesthesia
See also
  Status Clinical Trial Phase
Completed NCT02930928 - Can Habitus Adapted Length Based Body Weight Estimation be Improved by Adding Further Parameters?
Not yet recruiting NCT06281938 - Machine Learning and 3D Image-based Modeling for Body Weight Estimation. N/A