Trial · NCT02920060
Levetiracetam Versus Sodium Valproate in Children With Refractory Generalized Convulsive Status Epilepticus
NCT02920060, Phase 2, Completed, Banaras Hindu University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Levetiracetam Versus Sodium Valproate in Children With Refractory Generalized Convulsive Status Epilepticus. Trials, record NCT02920060. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02920060
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Levetiracetam Versus Sodium Valproate in Children With Refractory Generalized Convulsive Status Epilepticus
- NCT number
- NCT02920060
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 80 participants, actual
- Lead sponsor
- Banaras Hindu University
- Conditions
- Grand Mal Status Epilepticus
- Interventions
- Intravenous levetiracetam, Sodium valproate
- First posted
- 2016-09-30
- Last updated
- 2016-09-30
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | cessation of convulsions (clinically evident motor activity) | 30 minutes | clinical cessation of convulsions, vitals monitoring |
| Secondary | seizure activity at 24 hours of infusion | 24 hours | whether clinical convulsive activity cessation or not |
| Secondary | seizure recurrence | 24 hours | average number of seizure recurring after drug infusion within 24 hours |
| Secondary | additional number of drugs | 24 hours | number of additional drugs to control RSE within 24 hours of infusion |
| Secondary | time taken to control seizure activity | 24 hours | time needed to control convulsive activity from infusion time |
| Secondary | change in vital parameters after infusing interventional agent | 24 hours | vital parameters will be recorded every 15 minutes for the first 1 hour after the intervention began and mean value of vital parameters will be compared in two groups |
| Secondary | neurological outcome and seizure control | 1 month | to look for any neurological deficit or behavioural abnormality and seizure control at one month of follow-up |
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/NCT02920060
GET https://conductscience.org/api/trials/v1/NCT02920060/registered