Evaluating quality of life changes after epilepsy surgery
Comparison of Quality of Life and Changes Experienced by Patients After Epilepsy Surgery, With Long-term Epileptological Objective Results
This study looks at how epilepsy surgery has changed the quality of life for patients who had the procedure over two years ago.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 160 (estimated) |
| Ages | 15 Years and up |
| Sex | All |
| Sponsor | University Hospital, Toulouse Academic / other |
| Locations | 1 site (Toulouse) |
| Trial ID | NCT06035965 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on patients who have undergone epilepsy surgery at the Toulouse University Hospital more than two years ago. It aims to assess the quality of life and various changes experienced by these patients post-surgery using standardized questionnaires. The study will evaluate psychological, emotional, and cognitive impacts, as well as the effects on patients' social and professional lives. By gathering this data, the study seeks to provide insights into the long-term outcomes of epilepsy surgery.
Who should consider this trial
Good fit: Ideal candidates are patients who have had epilepsy surgery at least two years prior and are willing to participate in the research.
Not a fit: Patients under the age of 15, those with serious unrelated psychiatric conditions, or severe intellectual disabilities may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of the long-term benefits of epilepsy surgery, potentially guiding future treatment decisions.
How similar studies have performed: While there have been studies on epilepsy surgery outcomes, this specific focus on quality of life changes is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient operated in the context of epilepsy surgery dating back more than 2 years in the epileptology center of the Toulouse University Hospital. * Patient covered by a social security scheme. * Patient having given his non-objection to participate in the research. Exclusion Criteria: * Minor under the age of 15 at the time of the questionnaires. * Serious psychiatric pathology unrelated to epilepsy surgery. * Severe intellectual disability limiting responses to self-questionnaires. * Language barrier. * Patients under guardianship and protection of justice.
Where this trial is running
Toulouse
- CHU de Toulouse — Toulouse, France (Recruiting)
Study contacts
- Principal investigator: Helene Mirabel — University Hospital, Toulouse
- Study coordinator: Helene Mirabel
- Email: mirabel.h@chu-toulouse.fr
- Phone: 05 61 77 56 14
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.