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Epilepsy clinical trials

View clinical trials related to Epilepsy.

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NCT ID: NCT03994718 Completed - Epilepsy Clinical Trials

Creative Arts II Study

Start date: September 30, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the impact of music, visual art, or creative writing on quality of life measures for epilepsy patients.

NCT ID: NCT03958331 Completed - Epilepsy Clinical Trials

Behavioral Economics and Adherence in Teens (BEAT!)

Beat!
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

Non-adherence to antiepileptic drug therapy is a significant problem for adolescents with epilepsy and has a critical impact on health and patient-reported outcomes. Evidence-based adherence interventions are lacking in this population and are critically needed. This proposal seeks to develop and evaluate a mHealth social norms adherence intervention for adolescents with epilepsy.

NCT ID: NCT03953820 Completed - Epilepsy Clinical Trials

Diazepam Buccal Film (DBF) - Diastat Rectal Gel (DRG) Crossover Study

Start date: April 13, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This was a multiple centers, single-dose, open-label, randomized two-sequence crossover, two-period study to evaluate the pharmacokinetics (PK) of single doses of Diazepam Buccal Film (DBF) compared with Diastat® Rectal Gel (DRG) under fed conditions in adult male and female participants on a stable concomitant regimen of anti-epileptic drugs for the treatment of epilepsy.

NCT ID: NCT03953781 Completed - Epilepsy Clinical Trials

Effect of Valproate Versus Levetiracetam Monotherapy on Reproductive Functions in Epileptic Males

Start date: June 1, 2016
Phase:
Study type: Observational

Background: Different antiepileptic drugs are responsible for reproductive dysfunction in male epileptic patients. The aim of this study is to evaluate the effect of valproate versus levetiracetam as a monotherapy on males' sex hormones and sperm parameters in newly diagnosed epilepsy. Methods: This comparative study included 50 newly diagnosed epileptic male participants from outpatient clinic of Neurology department of Zagazig University Hospitals. All participants were subjected to complete general and neurological examination, Doppler ultrasonography of the testis, pre and post treatment serum sex hormone assay and semen analysis. Post- treatment re- evaluation check point was determined if eight weeks have passed after the last seizures. This study included two groups, group I: 25 participants, were treated by valproate (VPA) as a monotherapy till became seizure free at the last 8-weeks before post treatment check-point, with ages ranged from 18-43 years. Group II: 25 participants were treated by levetiracetam (LEV) with the same regimens of valproate as a monotherapy, with ages ranged from 20-45 years.

NCT ID: NCT03941613 Completed - Clinical trials for Epilepsy, Temporal Lobe

SEEG Guided RF-TC v.s. ATL for mTLE With HS

STARTS
Start date: August 5, 2019
Phase: N/A
Study type: Interventional

Mesial temporal lobe epilepsy (mTLE) is the most classical subtype of temporal lobe epilepsy, which is the indication of surgical intervention after evaluation. Until now, anterior temporal lobectomy (ATL) is still the recommended treatment for mTLE. However, evidences are accumulated including post ATL tetartanopia and memory deterioration and new minimized invasive treatments are introduced. Stereotactic EEG (SEEG) guided radio-frequency thermocoagulation (RF-TC) is one of the option with lower seizure freedom but with higher neurological function reservation. This study is aiming at comparison of the efficacy and safety between SEEG guided RF-TC and classical ATL in the treatment of mTLE.

NCT ID: NCT03939507 Completed - Epilepsy Clinical Trials

Outcome Study in Refractory Epilepsy (SOPHIE)

SOPHIE
Start date: November 6, 2006
Phase: N/A
Study type: Interventional

Over 1 million people in the European Union (EU) suffer from chronic refractory epilepsy. Their quality of life (QoL) is severely affected by seizures and by the adverse effect of antiepileptic drug (AED) treatment. Several new AEDs have been introduced in recent years, but their impact on the long-term outcome in these patients has been inadequately explored. Preliminary data from the U.S. suggests that using a standardize toll to quantitate adverse AED effects can improve outcome, but the general applicability of these findings is unclear. Objectives: 1) To assess prospectively AED utilization patterns in patients with refractory epilepsy ; 2) to assess how such treatments and other variables correlated with seizure control, adverse effects, and QoL in these patients; 3) to establish the impact of a standardized evaluation of adverse effects on clinical outcome. Methods: The project included a core observational study and a randomized intervention in a subcohort. In the core (observational) study, 1,000 consecutive refractory epilepsy patients were enrolled and followed-up prospectively at 10 centres in Italy. The following parameters were recorded at 0 (entry), 6, 12 and 18 months: (i) drug therapy; (ii) seizure frequency; (iii) adverse events based on medical examination and non-structured interview; (iii) treatment costs and, (iv) for patients above age 16, standardized questionnaires for adverse effects (AEP), depressive symptoms (Becks Depression Scale, BDS), QoL (QOLIE-31) and clinical global impression (CGI). The primary outcome (changes in QOLIE-31 scores) will be related to the other variables measured. In the randomized intervention, the subcohort meeting specific eligibility criteria (age >16 years, no progressive disorder, AEP score>=45 ) was randomized to two groups. In the intervention group, AEP score results were made available to the physician at each visit, while in the other group AEP scores were only made available at the end of follow-up. Primary outcome were changes in AEP score.

NCT ID: NCT03926273 Completed - Epilepsy Clinical Trials

Serum and Urine Ghrelin in Adult Epileptic Patients

Start date: June 1, 2018
Phase:
Study type: Observational

Several neuropeptides have concerned with epilepsy pathogenesis, ghrelin showed an anticonvulsant effect. There is a potential relation between its level and antiepileptic drugs (AED) response.

NCT ID: NCT03909984 Completed - Clinical trials for Epilepsy in Children

Promoting Implementation of Seizure Detection Devices in Epilepsy Care

PROMISE
Start date: April 26, 2018
Phase: N/A
Study type: Interventional

This is a multicenter home-based medical device intervention study, with prospective validation of the wearable seizure detection device (Nightwatch) and retrospective validation of remote sensors (video and audio detection) in children. The investigators will also perform a feasibility and utility analysis of Nightwatch.

NCT ID: NCT03896386 Completed - Epilepsy Clinical Trials

EPIDOGS Digital Seizure Diary for Owners of Alerting Dogs

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

During a three-month period, the study subjects will be using an electronic diary app that they can download and install on their smartphones to register the occurrence of seizures and also to register the potential alerting behaviour of their dogs. This information will increase the knowledge of the accuracy of these alerts.

NCT ID: NCT03879525 Completed - Depression Clinical Trials

EMR Outcomes: Anxiety and Depression in Epilepsy

Start date: December 16, 2019
Phase: N/A
Study type: Interventional

The purpose of this research is to find out how people with epilepsy and possible symptoms of anxiety or depression are doing for 6 months after a regular epilepsy clinic visit. Participants in this study will complete questionnaires either by phone or via the patient portal.