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NCT03065231
Lumbar Drain vs Extraventricular Drain to Prevent Vasospasm in Subarachnoid Hemorrhage
NA trial testing Extraventricular Drain in Vasospasm, Intracranial in 100 participants. Currently enrolling.
4 January 2027
Quick facts
| Lead sponsor | University of California, San Diego |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 100 |
| Start date | 1 January 2017 |
| Primary completion | 4 January 2027 |
| Estimated completion | 4 January 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Extraventricular Drain
- Lumbar Drain
Conditions studied
- Vasospasm, Intracranial — all drugs for Vasospasm, Intracranial →
- Subarachnoid Hemorrhage — all drugs for Subarachnoid Hemorrhage →
Sponsor
University of California, San Diego
Who can join
Adults 18 to 110, any sex, with Vasospasm, Intracranial or Subarachnoid Hemorrhage. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Vasospasm is a common complication after rupture of intracranial aneurysms causing devastating neurologic deficits and death. Vasospasm has been directly associated with the amount of subarachnoid blood inside the basal cisterns. Prior literature has attempted to refine treatment of ruptured intracranial aneurysms but does not have clear guidelines on the optimal method to drain subarachnoid blood. Two methods, extraventricular drain (EVD) and lumbar drain (LD) have been compared retrospectively yet remain controversial as to which method is optimal in reducing subarachnoid blood and preventing vasospasm. This study would be a prospective randomized trial in which patients would be assigned to EVD or LD and observed to see if one method of intervention is associated with preventing clinical vasospasm, decreasing subarachnoid blood, shortening overall ICU stay, and reducing the need for a permanent ventriculoperitoneal shunt. The conclusions of this study may identify an optimal treatment modality to benefit all future patients with ruptured intracranial aneurysms.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Targeting Hemoglobin to Reduce Delayed Cerebral Ischemia After Subarachnoid Hemorrhage.
Zeineddine HA, Honarpisheh P, McBride D, Pandit PKT, et al · · 2022 · cited 31× · PMID 35157256 · DOI 10.1007/s12975-022-00995-9 -
Delayed cerebral ischemia after aneurysmal subarachnoid hemorrhage: a narrative review.
Marques IP, Albuquerque CRC, Souza NVO, Andrade JBC, et al · · 2025 · cited 2× · PMID 40562372 · DOI 10.1055/s-0045-1809885
Verify or expand the search:
- PubMed search for NCT03065231
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Vasospasm, Intracranial
Currently open trials in the same condition.
- NCT04876638 — Minocycline for Aneurysmal Subarachnoid Hemorrhage (MASH) · Phase 2 · active not recruiting
Other University of California, San Diego trials
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03065231 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of California, San Diego
- Last refreshed: 4 March 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03065231.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing