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OpenTrials
Completed

NCT Number: NCT03814941

The Incidence of Artifacts in the Anesthesia Information Management System Database.

The purpose of the study is to evaluate the incidence of artifacts in the developed AIMS database

Completed

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Observational

Primary location

MacKay Memorial Hospital

Taipei, 104, Taiwan

About this study

At first, the authors evaluated the accuracy of the traditional, manually completed paper-based documentation, which sets a benchmark for the accuracy that the electronic documentation and database provides.

At the second portion, the investigators used the paper-based documentation as a standard to compare the electronic documentation. The incidence of artifact was double checked by two investigators.

At the third portion, the authors calculated the artifact incidence in the AIMS database, using paper based and electric document anesthesia records as the standard respectively.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patient undergo general or regional anesthesia
  • elective surgery

Exclusion criteria

  • emergency operation

Treatment and study plan

paper-based anesthesia record

Other

to evaluate the incidence of artifacts in the AIMS database by paper-based anesthesia record

electronic documents

Other

to evaluate the incidence of artifacts in the AIMS database by electronic documents anesthesia record

Primary outcomes

  1. percentage of artifacts

    Time frame: intraoperative (from the beginning to the end of anesthesia record)

    to evaluate how many percentage of artifacts for each of the included parameters

Secondary outcomes

  1. deviating values

    Time frame: intraoperative (from the beginning to the end of anesthesia record)

    to calculate the number of values deviating from the predefined baseline value

  2. percentage of devotional artifacts

    Time frame: intraoperative (from the beginning to the end of anesthesia record)

    to evaluate how many percentage of the deviations are artifacts

  3. episodes of artifacts

    Time frame: intraoperative (from the beginning to the end of anesthesia record)

    to find out the average of number of episodes across each artifact

  4. causes of artifacts

    Time frame: intraoperative (from the beginning to the end of anesthesia record)

    to find out the cause of the artifact and respective percentage

Sponsors and collaborators

Lead sponsor

Mackay Memorial Hospital

Other

Registry information

Official study title

To Evaluate the Incidence of Artifacts in the Locally Developed AIMS Database.

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jan 24, 2019
Registry last updated
Mar 15, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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