Last updated: 11/07/2018 17:25:49
Valproate monotherapy conversion to lamotrigine monotherapy efficacy assessment in open-label, prospective 32-week study in children 2 -12 aged with epilepsy. The LAM40090 Study Group.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Valproate monotherapy conversion to lamotrigine monotherapy efficacy assessment in open-label, prospective 32-week study in children 2 -12 aged with epilepsy. The LAM40090 Study Group.
Trial description: Valproate monotherapy conversion to lamotrigine monotherapy efficacy assessment in open-label, prospective 32-week study in children 2 -12 aged with epilepsy. The LAM40090 Study Group.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Abstract: valproate monotherapy conversion to lamotrigine monotherapy - efficacy assessment in open-iabel, prospective 32-week study in children aged 2 - 12 with epilepsy. the lam40090 study group . E. Szczepanik, A. Gniatkowska-Nowakowska M. Wierzbicki G. Sergot-Martynowska A. Terczynski 25th International Epilepsy Congress 10/12/2003 Lisbon; Portugal
Abstract: valproate monotherapy conversion to lamotrigine monotherapy - efficacy assessment in open-label, prospective 32-week study in children aged 2 - 12 with epilepsy. the lam40090 study group . Szczepanik, E, Gniatkowska-Nowakowska, A, Wierzbicki, M, Sergot-Martynowska, G, and Terczynski, A 5th European Congress on Epileptology 10/6/2002 Madrid; Spain
Szczepanik E., Gniatkowska-Nowakowska A., Wierzbicki M., Sergot-Martynowska G., Terczynski A. Epilepsia 2002;43 (Supplement 8):184.
Medical condition
Epilepsy
Product
lamotrigine
Collaborators
Not applicable
Study date(s)
December 1999 to July 2001
Type
Not applicable
Phase
4
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2001-02-07
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
Participate in clinical trial
Access to clinical trial data by researchers
Visit website