CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 318 enrolled
Drug / intervention
Quality of preoperative information register +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04259268
NCT04259268N/ACompleted

Evaluation of the Quality of Preoperative Information Obtained Through Preanestes@s, a Web Based Application: Paired Comparison of a Web Based Questionnaire, a Virtual Non Face to Face Assessment and Outpatient Visit

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla·observational·Posted Feb 6, 2020·Updated May 26, 2021

In Brief

An observational study evaluating Quality of preoperative information register and Suitability of information contained in the informed consent for Mobile Applications and 2 related conditions. Completed, enrolled 318 participants across 1 site.

Detailed Summary

In this prospective and paired study, the investigators evaluate whether the preoperative information recorded through a web based questionnaire together with a virtual non face to face patient assessment based on the information recorded by the questionnaire and the electronic records of patients is of a comparable quality to that obtained with the traditional outpatient interview.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesSpain
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedFeb 6, 2020
Enrollment StartFeb 7, 2020
Primary CompletionMar 31, 2021
Study CompletionMay 25, 2021
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 6.4 years ago

Interventions

Quality of preoperative information registerother

Register of principal (grade ASA classification) and secondary variables (allergies, antiplatelet or blood thinners prescriptions, cardiovascular diseases, present medication)

Suitability of information contained in the informed consentother

Register of information regarding specific individual risks and personal data (patient and doctor identification and signature)