Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03814941
Other study ID # 19MMHIS017e
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2021
Est. completion date December 31, 2022

Study information

Verified date March 2023
Source Mackay Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 31, 2022
Est. primary completion date July 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - patient undergo general or regional anesthesia - elective surgery Exclusion Criteria: - emergency operation

Study Design


Related Conditions & MeSH terms

  • Artifacts
  • Integrated Advanced Information Management Systems

Intervention

Other:
paper-based anesthesia record
to evaluate the incidence of artifacts in the AIMS database by paper-based anesthesia record
electronic documents
to evaluate the incidence of artifacts in the AIMS database by electronic documents anesthesia record

Locations

Country Name City State
Taiwan MacKay Memorial Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
Mackay Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (3)

Hoorweg AJ, Pasma W, van Wolfswinkel L, de Graaff JC. Incidence of Artifacts and Deviating Values in Research Data Obtained from an Anesthesia Information Management System in Children. Anesthesiology. 2018 Feb;128(2):293-304. doi: 10.1097/ALN.0000000000001895. — View Citation

Kool NP, van Waes JA, Bijker JB, Peelen LM, van Wolfswinkel L, de Graaff JC, van Klei WA. Artifacts in research data obtained from an anesthesia information and management system. Can J Anaesth. 2012 Sep;59(9):833-41. doi: 10.1007/s12630-012-9754-0. Epub 2012 Jul 18. — View Citation

Wilbanks BA, Berner ES, Alexander GL, Azuero A, Patrician PA, Moss JA. The effect of data-entry template design and anesthesia provider workload on documentation accuracy, documentation efficiency, and user-satisfaction. Int J Med Inform. 2018 Oct;118:29-35. doi: 10.1016/j.ijmedinf.2018.07.006. Epub 2018 Jul 24. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of artifacts to evaluate how many percentage of artifacts for each of the included parameters intraoperative (from the beginning to the end of anesthesia record)
Secondary deviating values to calculate the number of values deviating from the predefined baseline value intraoperative (from the beginning to the end of anesthesia record)
Secondary percentage of devotional artifacts to evaluate how many percentage of the deviations are artifacts intraoperative (from the beginning to the end of anesthesia record)
Secondary episodes of artifacts to find out the average of number of episodes across each artifact intraoperative (from the beginning to the end of anesthesia record)
Secondary causes of artifacts to find out the cause of the artifact and respective percentage intraoperative (from the beginning to the end of anesthesia record)
See also
  Status Clinical Trial Phase
Completed NCT04448600 - Bone Conduction Implant and MRI