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NCT00614549

Long-term Evaluation of the Efficacy and Safety of Levetiracetam in Routine Clinical Practice in the Czech and Slovak Republics, Hungary, and Romania - Non-interventional Study

Completed Last updated 25 May 2012
What this trial tests

trial in Epilepsy in 2,569 participants. Completed in 1 June 2009.

Timeline
1 March 2007
Primary endpoint
1 June 2009
1 June 2009

Quick facts

Lead sponsorUCB Pharma
StatusCompleted
Study typeOBSERVATIONAL
Enrollment2,569
Start date1 March 2007
Primary completion1 June 2009
Estimated completion1 June 2009

Conditions studied

Sponsor

UCB Pharma — full company profile →

Who can join

4 and older, any sex, with Epilepsy. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

To evaluate, over 1 year period, the efficacy and safety of newly prescribed levetiracetam as add-on treatment (POS, myoclonoc seizures in JME and PGTCS in IGE) or primary monotherapy (partial onset seizures) in adult and paediatric patients within the approved age limits in routine clinical practice in Czech and Slovak Republics, Hungary, and Romania. Non-interventional study.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Epilepsy

Currently open trials in the same condition.

Other UCB Pharma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00614549.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing