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Study to Improve the Treatment of Epilepsy (SITE)

Primary Purpose

Epilepsy

Status
Unknown status
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
All registered antiepileptic drugs
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epilepsy focused on measuring epilepsy, antiepileptic drugs, side effects, quality of life

Eligibility Criteria

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

Inclusion Criteria: Aged 18 years or older Treatment: antiepileptic drugs for epilepsy No change in medication during last 6 months No obvious clinical reason to change medication immediately Exclusion Criteria: Concurrent disease or disorder that might interfere with the conduct of the study Inability to comply to the protocol Impaired intellectual functioning, leading to inability to comply to the protocol and complete the necessary questionnaires

Sites / Locations

  • AZM
  • Catharina Hospital
  • Hospital Gooi-Noord
  • Oosterschelde Hospital
  • MCRZ
  • MC Haaglanden

Outcomes

Primary Outcome Measures

Complaints (questionnaire) at 7 and 13 months

Secondary Outcome Measures

Quality of Life (Qolie-10) at 7 and 13 months

Full Information

First Posted
August 17, 2005
Last Updated
October 20, 2005
Sponsor
UMC Utrecht
Collaborators
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT00133081
Brief Title
Study to Improve the Treatment of Epilepsy (SITE)
Official Title
Study to Improve the Treatment of Epilepsy (SITE). A Randomized Study Comparing Adjustment of Treatment to Reduce Side Effects of Antiepileptic Drugs With Continuing Treatment Unchanged
Study Type
Interventional

2. Study Status

Record Verification Date
March 2004
Overall Recruitment Status
Unknown status
Study Start Date
October 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
UMC Utrecht
Collaborators
GlaxoSmithKline

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to assess whether changing antiepileptic medication can reduce side effects and improve the quality of life in patients with epileptic seizures that are well controlled with antiepileptic drugs.
Detailed Description
Background. The aim of the treatment with antiepileptic drugs (AEDs) is to achieve seizure freedom without causing side effects. Assessment of side effects is difficult. They may start insidiously, the patient may not associate certain complaints with the use of AEDs, or the treating physician does not take enough time to discuss this topic during the limited time of a visit in the outpatient department. We know from clinical trials that side effects occur in a substantial group of patients. We do not know whether we deal with this possible complication in an adequate way in clinical practice. Study objective. To study whether adjustment of medication will reduce the occurrence of side effects and improve quality of life. Study design. A randomised clinical trial comparing adjustment of treatment in case of relevant side effects to continuing treatment unchanged. Relevant side effects are defined as at least one moderate or serious problem scored on a questionnaire to assess complaints in people with epilepsy. Patients who do not report relevant side effects will be followed for 13 months (arm A) in which two visits are scheduled, after 7 and 13 months respectively. The patients who do report relevant side effects will be randomised to either discussion of the questionnaire results and adjustment of treatment if appropriate (arm B) or to ignore the results of the questionnaire and continue treatment unchanged (arm C). Investigations will be repeated in both groups after 7 and 13 months after the initial visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy
Keywords
epilepsy, antiepileptic drugs, side effects, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
255 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
All registered antiepileptic drugs
Primary Outcome Measure Information:
Title
Complaints (questionnaire) at 7 and 13 months
Secondary Outcome Measure Information:
Title
Quality of Life (Qolie-10) at 7 and 13 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 years or older Treatment: antiepileptic drugs for epilepsy No change in medication during last 6 months No obvious clinical reason to change medication immediately Exclusion Criteria: Concurrent disease or disorder that might interfere with the conduct of the study Inability to comply to the protocol Impaired intellectual functioning, leading to inability to comply to the protocol and complete the necessary questionnaires
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cees A van Donselaar, MD PhD
Organizational Affiliation
UMC Utrecht
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sabine G Uijl, MSc
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Albert P Aldenkamp, PhD
Organizational Affiliation
AZM Maastricht
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Cuno SP Uiterwaal, PhD
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
Facility Information:
Facility Name
AZM
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6202 AZ
Country
Netherlands
Facility Name
Catharina Hospital
City
Eindhoven
State/Province
Noord Brabant
ZIP/Postal Code
5623 EJ
Country
Netherlands
Facility Name
Hospital Gooi-Noord
City
Blaricum
State/Province
Noord Holland
ZIP/Postal Code
1250 CA
Country
Netherlands
Facility Name
Oosterschelde Hospital
City
Goes
State/Province
Zeeland
ZIP/Postal Code
4460 BB
Country
Netherlands
Facility Name
MCRZ
City
Rotterdam
State/Province
Zuid Holland
ZIP/Postal Code
3007 AC
Country
Netherlands
Facility Name
MC Haaglanden
City
The Hague
State/Province
Zuid Holland
ZIP/Postal Code
2512 VA
Country
Netherlands

12. IPD Sharing Statement

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Study to Improve the Treatment of Epilepsy (SITE)

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