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Descriptive Study to Evaluate the Understanding Degree of Informed Consent in Surgical Procedures

NCT03960723 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2023-09-25

No results posted yet for this study

Summary

The Informed Consent (IC) of a medical procedure is the aceptation of a diagnostic or therapeutic procedure by the patient, after receiving the necessary and accurate information about it. Freedom, information and understanding have to be the main requirements in this proccess.

The main goal of this study is to assess if patients that are going to be operated at Hospital de la Santa Creu i Sant Pau in the CSI (Surgery without previous hospitalization) unit, really understood the information about the procedure.

Conditions

  • Informed Consent

Interventions

OTHER

Questionnaire

A questionnaire asking the patients for several questions related to the Informed Consent Form they have signed before surgery, will be administered.

Sponsors & Collaborators

  • Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

    lead OTHER

Principal Investigators

  • Rosa Mª Antonijoan Arbos, MD, PhD · Institut de Recerca de l´Hospital de la Santa Creu i Sant Pau

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-09
Primary Completion
2019-12-09
Completion
2019-12-09

Countries

  • Spain

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 NCT03960723 on ClinicalTrials.gov