CClinicalTrials.gg
CompletedNCT01115959Updated Jun 12, 2014

Seizures Post Intracerebral Hemorrhage

A Phase 4 interventional study of valproic acid and placebo bid in Post Cerebral Hemorrhage, sponsored by Wolfson Medical Center. Completed. Per ClinicalTrials.gov, last updated 2014-06-12.

Sponsored by Wolfson Medical Center · Phase 4, Interventional, and Prevention

Phase
Phase 4
Study type
Interventional
Enrollment
72
Allocation
Randomized
Sex
All
01

Study summary

This study examines early antiepileptic treatment with valproic acid for acute cerebral hemorrhage against a placebo group immediately post event to evaluate the outcome of these patients regarding seizures and neurological outcome.

02

Conditions studied

  • Post Cerebral Hemorrhage
03

In context

Cerebral Hemorrhage

476 studies on the registry are indexed under Cerebral Hemorrhage; 181 are open to participants now.

This study's enrollment of 72 is below the median of 100 across 287 interventional studies indexed under Cerebral Hemorrhage.

Browse Cerebral Hemorrhage studies →

Lead sponsor

Wolfson Medical Center is the lead sponsor of 113 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • cerebral hemorrhage spontaneous

Exclusion criteria

Exclusion Criteria:

  • early seizures
05

Study design

Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
72 participants (actual)

Study arms

  • Active comparator
    valproic acid

    Valproic acid given orally 400mg twice daily

    Drug: valproic acid · Drug: placebo bid

  • Placebo comparator
    placebo

    Placebo twice daily for one month

    Drug: placebo bid

Interventions

  • Drugvalproic acid

    treatment of 1 month dosage of 400 mg BID

  • Drugplacebo bid
06

What researchers measure

Primary outcomes

  1. number of seizures

    Time frame: study drug for 1 month and 1 year follow up

Secondary outcomes

  1. neurological outcome NIHSS

    Time frame: during 1 month study drug and 1 year post follow up

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01115959
Lead sponsor
Wolfson Medical Center
Responsible party
Dr. Yair Lampl (Professor Yair Lampl, Wolfson Medical Center) — Principal investigator
First posted
May 4, 2010
Start date
Feb 2003
Primary completion
Oct 2008
Completion
Dec 2008
Last update
Jun 12, 2014

Study contacts

ronit gilad, md
principal investigator · E Wolfson med center
ronit gilad, md
principal investigator · E wofson med center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2010. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion