Clinical Trials Directory

Trials / Terminated

TerminatedNCT00376766

Clinical Trial : TROCC (Quick Oral Treatment of Cluster Epileptic Seizures)

Rapid Oral Treatment of Cluster Epileptic Seizures. Efficacy Assessment of Levetiracetam in Cluster Seizures.

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
112 (estimated)
Sponsor
University Hospital, Grenoble · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is a double blind, placebo controlled, add-on clinical trial, of levetiracetam efficacy and safety, in epilepsy cluster seizure. Efficacy is evaluated in the range of 2 to 24 hours after taking the tablet. If the patient has a seizure during this interval, he is considered as a non-respondent patient.

Detailed description

Seizure clustering has been defined as a series of unusual frequency of seizures with return to baseline between events. The most common definition of cluster seizure is three seizures per 24 hours. The usual treatment of cluster seizure is benzodiazepin. This is recognized efficient therapy but has many side effects. Thus it is important to develop as an new therapeutic to improve patient care. Levetiracetam is an antiepileptic drug used in addition to other antiepileptic drugs with less side effects than benzodiazepin. The aim of this study is to evaluate the effectiveness and safety of levetiracetam in epilepsy cluster seizure. This is a double blind, placebo controlled, add-on clinical trial with two phases : Phase 1 : Double blind phase during 24 hours (H0 to H24). After consent signature and randomization, the patient takes two tablets of levetiracetam or placebo. If the patient has a seizure between H3 and H24, he is considered as a non-respondent patient. If there is a risk of rapid evolution to an statue epilepticus, the investigator can break the blind and adapt the patient treatment accordingly. Phase 2 : This is an open phase after H24. this phase consists of breaking the blind with free adaption of the therapy by the investigator, and patients follow-up during 1 month. The randomization is stratify by center. The size of randomization blocks is random because of the systematic breaking blind after 24 hours.

Conditions

Interventions

TypeNameDescription
DRUGlevetiracetam

Timeline

Start date
2007-02-01
Primary completion
2008-04-01
Completion
2008-04-01
First posted
2006-09-15
Last updated
2015-05-28

Locations

10 sites across 1 country: France

Source: ClinicalTrials.gov record NCT00376766. Inclusion in this directory is not an endorsement.