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Evaluation of an Algorithm for Length Based Weight Estimation in Comparison to Known Devices

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Weight-Estimation

Treatments

Device: Accuracy of an algorithm and the Broselow Tape

Study type

Observational

Funder types

Other

Identifiers

NCT02620540
KEK-ZH-Nr. 2015-0191 - Part 2

Details and patient eligibility

About

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.

Full 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.

Enrollment

312 patients

Sex

All

Ages

1 day to 16 years old

Volunteers

Accepts Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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