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Evaluation of Digital, Telephonic and Conventional Consent for Anaesthesia

NCT04701450 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2023-10-24

No results posted yet for this study

Summary

In this study, the investigators aim to evaluate patient satisfaction between three methods of obtaining informed consent for anaesthesia. Patients are asked to partake in a short survey after being informed about the anaesthetic procedure either conventionally in the anesthesia department, telephonically or digitally.

Conditions

  • Patient Satisfaction

Interventions

OTHER

digital consent

the patient's medical history is taken in a digital survey, information about the anaesthetic procedure is aided by video material

Sponsors & Collaborators

  • Medical University of Vienna

    lead OTHER

Principal Investigators

  • David M. Baron, MD · Medical University of Vienna

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-12-01
Primary Completion
2022-12-31
Completion
2022-12-31

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04701450 on ClinicalTrials.gov