Trial · NCT02876289
Retrospective Evaluation of Perampanel in a French Neurology and Epileptology Department (Hospices Civil de Lyon)
NCT02876289, Completed, Hospices Civils de Lyon
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Retrospective Evaluation of Perampanel in a French Neurology and Epileptology Department (Hospices Civil de Lyon). Trials, record NCT02876289. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02876289
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Retrospective Evaluation of Perampanel in a French Neurology and Epileptology Department (Hospices Civil de Lyon)
- NCT number
- NCT02876289
- Status
- Completed
- Enrollment
- 110 participants, actual
- Lead sponsor
- Hospices Civils de Lyon
- Conditions
- Refractory Epilepsy
- Interventions
- Perampanel
- First posted
- 2016-08-23
- Last updated
- 2016-08-24
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Retention rate | 6 months | Proportion of patient still treated with Perampanel 6 months after its initiation |
| Secondary | Retention rate | 12 months | Proportion of patients still treated with Perampanel 12 months after its initiation |
| Secondary | Seizure freedom | 6 months | Proportion of seizure-free patients during at least 6 months |
| Secondary | Responder rates | 6 months | Responder rates is defined as a reduction in seizure frequency of 50% or more compared with the three months before the initiation of perampanel. |
| Secondary | Responder rates | 12 months | Responder rates is defined as a reduction in seizure frequency of 50% or more compared with the three months before the initiation of perampanel. |
| Secondary | Total withdrawal rate | 6 months | Discontinuation rates at 6 months due to inefficiency or adverse effects |
| Secondary | Total withdrawal rate | 12 months | Discontinuation rates at 12 months due to inefficiency or adverse effects |
| Secondary | Observed adverse effects during the observation period | 12 months |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02876289
GET https://conductscience.org/api/trials/v1/NCT02876289/registered