Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06792383

Psychological and Psychiatric Assessment in Patients Eligible for Epilepsy Surgery

Led by Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta · Updated on 2026-02-12

180

Participants Needed

1

Research Sites

312 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the study is to describe the socio-demographic, clinical, psychological, and psychiatric characteristics of patients with drug-resistant focal epilepsy eligible for epilepsy surgery and any changes in these parameters over time after surgery. Additionally, the study seeks to describe the levels of quality of life, dissociative experiences, prevalence of various psychiatric symptoms, irritability, depressive symptoms, anxiety symptoms, and stigma perception in patients with drug-resistant focal epilepsy eligible for epilepsy surgery and any changes over time after surgery.

CONDITIONS

Official Title

Psychological and Psychiatric Assessment in Patients Eligible for Epilepsy Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 or older at the time of enrollment
  • Patients with drug-resistant focal epilepsy followed at the Institute for at least 6 months
  • Patients with drug-resistant focal epilepsy eligible for epilepsy surgery
  • Patients capable of providing informed consent to participate in the study and for the processing of personal data
Not Eligible

You will not qualify if you...

  • Patients with evident and/or diagnosed cognitive or psychiatric disorders that prevent participation in an interview, proper understanding of informed consent, or completion of questionnaires

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Foundation IRCCS Carlo Besta Neurological Institute

Milan, Italy, 20133

Actively Recruiting

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Research Team

R

Rui Quintas, PsyD

CONTACT

M

Marco de Curtis, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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