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

Primary Purpose

Epilepsy, Drug Resistant

Status
Terminated
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
levetiracetam
Sponsored by
University Hospital, Grenoble
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epilepsy focused on measuring Cluster seizure, seizure clustering, repetitive seizure, Drug resistant epilepsy, Levetiracetam, keppra

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age from 18 to 65
  • Drug resistant epilepsy, partial seizure
  • Epilepsy diagnosed for more than 2 years
  • Epilepsy treated for more than 1 year with no change of treatment in the month before the enrolment
  • Onset of cluster seizure in the 24 hours before enrolment
  • For women : effective contraception
  • Affiliation to the French social security

Exclusion Criteria:

  • Inability to tolerate levetiracetam, likely poor compliance
  • Patient taking antiepileptic treatment (benzodiazepine) in addition to current treatment during the last 48h00.
  • Patient taking 1g/day of levetiracetam with Creatinin clearance < 50ml/min
  • Patient taking 2g/day of levetiracetam with Creatinin clearance < 80ml/min
  • Patient taking more than 2g/day of levetiracetam
  • Hepatic or cardiovascular pathology
  • Progressive psychiatric pathology
  • Degenerative neurologic disease
  • Cluster seizure due to an acute symptomatic reason
  • Disorder of consciousness
  • Suspicion of status epilepticus or rapid evolution to status epilepticus
  • Suspicion of psychogenic nonepileptic seizure
  • Pregnant woman or nursing woman
  • Suicidal thoughts
  • Incapacity to give consent, minor patient

Sites / Locations

  • Neurology department
  • Etablissement la Teppe
  • Neurology department
  • Neurology department
  • Neurology department
  • Neurology department
  • Neurology department
  • Neurology Department
  • Neurology department
  • Neurology department

Outcomes

Primary Outcome Measures

Ratio of patients who are free of seizure between H3 and H24 in both groups.

Secondary Outcome Measures

Items 1,2,3 of the Clinical Global Impression scale.
Side effects during the study.
Time between H0 and the last seizure.
Type and ratio of epileptic fit between H0 and H24.
Number of seizures occured between H3 and H10, H10 and H17, H17 and H24, corresponding to the half-time of the treatment (7 hours).
Description of therapeutic adaptation at 1 month after patient enrolment.

Full Information

First Posted
September 14, 2006
Last Updated
May 27, 2015
Sponsor
University Hospital, Grenoble
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, UCB Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT00376766
Brief Title
Clinical Trial : TROCC (Quick Oral Treatment of Cluster Epileptic Seizures)
Official Title
Rapid Oral Treatment of Cluster Epileptic Seizures. Efficacy Assessment of Levetiracetam in Cluster Seizures.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Terminated
Why Stopped
recruitment recruitment recruitment recruitment difficulties
Study Start Date
February 2007 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
April 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, UCB Pharma

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy, Drug Resistant
Keywords
Cluster seizure, seizure clustering, repetitive seizure, Drug resistant epilepsy, Levetiracetam, keppra

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
112 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
levetiracetam
Primary Outcome Measure Information:
Title
Ratio of patients who are free of seizure between H3 and H24 in both groups.
Secondary Outcome Measure Information:
Title
Items 1,2,3 of the Clinical Global Impression scale.
Title
Side effects during the study.
Title
Time between H0 and the last seizure.
Title
Type and ratio of epileptic fit between H0 and H24.
Title
Number of seizures occured between H3 and H10, H10 and H17, H17 and H24, corresponding to the half-time of the treatment (7 hours).
Title
Description of therapeutic adaptation at 1 month after patient enrolment.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age from 18 to 65 Drug resistant epilepsy, partial seizure Epilepsy diagnosed for more than 2 years Epilepsy treated for more than 1 year with no change of treatment in the month before the enrolment Onset of cluster seizure in the 24 hours before enrolment For women : effective contraception Affiliation to the French social security Exclusion Criteria: Inability to tolerate levetiracetam, likely poor compliance Patient taking antiepileptic treatment (benzodiazepine) in addition to current treatment during the last 48h00. Patient taking 1g/day of levetiracetam with Creatinin clearance < 50ml/min Patient taking 2g/day of levetiracetam with Creatinin clearance < 80ml/min Patient taking more than 2g/day of levetiracetam Hepatic or cardiovascular pathology Progressive psychiatric pathology Degenerative neurologic disease Cluster seizure due to an acute symptomatic reason Disorder of consciousness Suspicion of status epilepticus or rapid evolution to status epilepticus Suspicion of psychogenic nonepileptic seizure Pregnant woman or nursing woman Suicidal thoughts Incapacity to give consent, minor patient
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louis Maillard, Dr
Organizational Affiliation
Central Hospital, Nancy, France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Serge CHASSAGNON, Dr
Organizational Affiliation
University Hospital of Strasbourg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Cecile SABOURY, Dr
Organizational Affiliation
University Hospital of Strasbourg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Edouard HIRSH, Dr
Organizational Affiliation
University Hospital of Strasbourg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
William SZHURAJ, Dr
Organizational Affiliation
University Hospital of Lille
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philippe DERAMBURE, Dr
Organizational Affiliation
University Hospital of Lille
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jerome PETIT, Dr
Organizational Affiliation
La Teppe Institution
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vincent TAREL, Dr
Organizational Affiliation
Regional Hospital of Chambery
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dominique ROSENBERG, Dr
Organizational Affiliation
University Hospital, Clermont-Ferrand
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Helene CATENOIX, Dr
Organizational Affiliation
University Hospital of Lyon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philippe RYVELIN, Dr
Organizational Affiliation
University Hospital of Lyon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philippe CONVERS, Dr
Organizational Affiliation
University Hospital of St Etienne
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pierre THOMAS, Dr
Organizational Affiliation
University Hospital of Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neurology department
City
Nice
State/Province
Alpes de Haute provence
ZIP/Postal Code
06002
Country
France
Facility Name
Etablissement la Teppe
City
Tain l'Hermitage
State/Province
Drome
ZIP/Postal Code
26600
Country
France
Facility Name
Neurology department
City
Grenoble
State/Province
Isere
ZIP/Postal Code
3043
Country
France
Facility Name
Neurology department
City
St Etienne
State/Province
Loire
ZIP/Postal Code
42055
Country
France
Facility Name
Neurology department
City
Lille
State/Province
Nord
ZIP/Postal Code
59037
Country
France
Facility Name
Neurology department
City
Clermont-Ferrand
State/Province
Puy de Dome
ZIP/Postal Code
63003
Country
France
Facility Name
Neurology department
City
Lyon
State/Province
Rhone
ZIP/Postal Code
69000
Country
France
Facility Name
Neurology Department
City
Chambery
State/Province
Savoie
ZIP/Postal Code
73000
Country
France
Facility Name
Neurology department
City
Nancy
ZIP/Postal Code
54035
Country
France
Facility Name
Neurology department
City
Strasbourg
ZIP/Postal Code
67091
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
15660781
Citation
Haut SR, Shinnar S, Moshe SL. Seizure clustering: risks and outcomes. Epilepsia. 2005 Jan;46(1):146-9. doi: 10.1111/j.0013-9580.2005.29004.x.
Results Reference
background
PubMed Identifier
9637805
Citation
Dreifuss FE, Rosman NP, Cloyd JC, Pellock JM, Kuzniecky RI, Lo WD, Matsuo F, Sharp GB, Conry JA, Bergen DC, Bell WE. A comparison of rectal diazepam gel and placebo for acute repetitive seizures. N Engl J Med. 1998 Jun 25;338(26):1869-75. doi: 10.1056/NEJM199806253382602.
Results Reference
background
PubMed Identifier
10565590
Citation
Mitchell WG, Conry JA, Crumrine PK, Kriel RL, Cereghino JJ, Groves L, Rosenfeld WE. An open-label study of repeated use of diazepam rectal gel (Diastat) for episodes of acute breakthrough seizures and clusters: safety, efficacy, and tolerance. North American Diastat Group. Epilepsia. 1999 Nov;40(11):1610-7. doi: 10.1111/j.1528-1157.1999.tb02047.x.
Results Reference
background
PubMed Identifier
10999557
Citation
Shorvon SD, Lowenthal A, Janz D, Bielen E, Loiseau P. Multicenter double-blind, randomized, placebo-controlled trial of levetiracetam as add-on therapy in patients with refractory partial seizures. European Levetiracetam Study Group. Epilepsia. 2000 Sep;41(9):1179-86. doi: 10.1111/j.1528-1157.2000.tb00323.x.
Results Reference
background
PubMed Identifier
10908898
Citation
Cereghino JJ, Biton V, Abou-Khalil B, Dreifuss F, Gauer LJ, Leppik I. Levetiracetam for partial seizures: results of a double-blind, randomized clinical trial. Neurology. 2000 Jul 25;55(2):236-42. doi: 10.1212/wnl.55.2.236.
Results Reference
background

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

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