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Lumbar Drain With Intrathecal Nicardipine in Aneurysmal Subarachnoid Hemorrhage

StatusNot Yet Recruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 1 year 1 month later across 2 updates Jan 2027 → Mar 2028
See other at-risk trials from Wake Forest University Health Sciences

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary and study completion pushed from Mar 2027 to Mar 2028
    • Start date: Sep 2026 to Jan 2027
    • Eligibility criteria expanded, about 12 words
    • Secondary endpoints: details revised at 1 of 2 entries
  2. Start date: Jun 2026 to Sep 2026
    • Primary and study completion pushed from Jan 2027 to Mar 2027
    v5
  3. Start date: Apr 2026 to Jun 2026v4
  4. Start date: Feb 2026 to Apr 2026v3
  5. Start date: Jan 2026 to Feb 2026v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to determine the effectiveness of prophylactic administration of intra-thecal nicardipine though lumbar cerebrospinal fluid drain in prevention of symptomatic vasospasm in patients with subarachnoid hemorrhage due to rupture of cerebral aneurysms.
Trial Details
NCT Number NCT07246629
Lead Sponsor Wake Forest University Health Sciences
Conditions
(from sponsor)		 Subarachnoid Hemorrhage
Related terms Intracranial Aneurysm, Subarachnoid Hemorrhage
Enrollment 214 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov