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Episodic Memory Before and After Surgery in Drug-resistant Partial Epilepsies (MemO-Epi)

I

Institut National de la Santé Et de la Recherche Médicale, France

Status

Unknown

Conditions

Memory Impairment
Epilepsy, Unspecified, Pharmacologically Resistant

Treatments

Other: No intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT01919957
C12-11
2013-A00343-42 (Registry Identifier)

Details and patient eligibility

About

This study has two purposes: firstly, a better understanding of the neurobiological processes underlying episodic memory and, secondly, the development of useful clinical applications for epileptic patients, in particular the prediction of postoperative memory deficits and the development of cognitive remediation therapies.

Memory performances during a fMRI experiment will be assessed in controls and epileptic patients before and after the surgery.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with drug-resistant epilepsy
  • Age of 18 years or more
  • Follow-up in the epilepsy unit at Pitié-Salpêtrière Hospital
  • Before or after the presurgical evaluation unit including a video-EEG monitoring, a structural brain imaging and a full neuropsychological assessment
  • Covered by a social security system
  • Signing of consent form

Exclusion criteria

  • Persons under guardianship, curatorship or any other administrative or judicial deprivation of rights and freedom
  • Refusal to consent form
  • Contraindications to MRI
  • Pregnancy
  • Refusal to be informed in the case of detection of an abnormality during the experiment

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

120 participants in 1 patient group

memory outcome
No Intervention group
Treatment:
Other: No intervention

Trial contacts and locations

1

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Central trial contact

Virginie LAMBRECQ, MD; Sophie DUPONT, MD, PhD

Data sourced from clinicaltrials.gov

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