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NCT06792383Recruiting

Psychological and Psychiatric Assessment in Patients Eligible for Epilepsy Surgery

Source: ClinicalTrials.gov · Last updated 12 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
180 (estimated)
First submitted
8 Jan 2025
Start date
2 Dec 2020
Primary completion date
Dec 2026
Lead sponsor
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Diseases
Epilepsy
NCT number
NCT06792383

What you commit to

  • Study type: Interventional
  • Planned participants: 180
  • From 2 Dec 2020 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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.

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Foundation IRCCS Carlo Besta Neurological Institute
Coordinator of this site? Confirm its status
MilanItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.