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NCT06119061 · ClinicalTrials.gov registry record · Phase 4
Telavancin Blood and Cerebrospinal Fluid Concentrations in Patients With External Ventricular Drainage
A Phase 4 study of Subarachnoid Hemorrhage, Aneurysmal, sponsored by Aaron Cook.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT06119061: Recruiting Phase 4 study of Subarachnoid Hemorrhage, Aneurysmal, sponsored by Aaron Cook.
NCT06119061 is a Phase 4 study of Subarachnoid Hemorrhage, Aneurysmal that is actively recruiting participants, run by Aaron Cook. The registered enrollment target is 20 participants, below the 161-participant average among 8 other Subarachnoid Hemorrhage, Aneurysmal trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06119061, a Phase 4 study of Subarachnoid Hemorrhage, Aneurysmal, is actively recruiting participants, sponsored by Aaron Cook.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The proposed study aims to evaluate the CNS penetration of telavancin in a critically ill population using cerebrospinal fluid (CSF) drawn from external ventricular drains (EVDs). Patients with EVDs were chosen as the target population because they frequently require prolonged admission to the intensive care unit and drainage of CSF in order to prevent hydrocephalus. The estimated sample size is 20 subjects. This is a prospective cohort of patients with SAH. Patients will be included if they have an in-dwelling EVD, aged 18-85 years old. Subjects will receive telavancin 10mg/kg (maximum 1000mg) every 24 hours for 3 consecutive doses. Serial serum and CSF samples will be obtained. An 8-hour urine collection will be completed on study day 2 in order to define the patient's measured creatinine clearance.
Primary Outcome
Telavancin concentrations in CSF drawn from external ventricular drains will be compared to samples from the serum to determine the degree to which telavancin is present in the CNS
Conditions Studied
Interventions
- DRUG Telavancin Injection
Study Locations (1)
Kentucky
- University of Kentucky - Lexington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2024-07-02 |
| Est. Completion | 2026-12 |
| Phase | Phase 4 |
What NCT06119061 shows while recruiting
NCT06119061 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 161-participant average among 8 other Subarachnoid Hemorrhage, Aneurysmal trials with a reported enrollment target (88% lower).
The record links to 1 condition, with Subarachnoid Hemorrhage, Aneurysmal appearing as the primary indexed condition, and to 1 intervention - of which Telavancin Injection is the first listed.
NCT06119061 reports a single indexed study location in Kentucky.
Frequently Asked Questions
What is clinical trial NCT06119061 about?
NCT06119061 is a clinical study titled "Telavancin Blood and Cerebrospinal Fluid Concentrations in Patients With External Ventricular Drainage". The proposed study aims to evaluate the CNS penetration of telavancin in a critically ill population using cerebrospinal fluid (CSF) drawn from external ventricular drains (EVDs). Patients with EVDs were chosen as the target population because they frequently require prolonged admission to the inten...
What is the current status of trial NCT06119061?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2024-07-02. Estimated completion is 2026-12.
What conditions does trial NCT06119061 study?
This clinical trial studies the following conditions: Subarachnoid Hemorrhage, Aneurysmal.
What interventions are being tested in trial NCT06119061?
The interventions under investigation include: Telavancin Injection (DRUG).
Who is sponsoring clinical trial NCT06119061?
This trial is sponsored by Aaron Cook, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06119061 being conducted?
This trial has 1 study location across Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Subarachnoid Hemorrhage, Aneurysmal
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06119061's enrollment target sits among peer trials
20 5th of 8 higher than 3 of 8 other Subarachnoid Hemorrhage, Aneurysmal trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Subarachnoid Hemorrhage, Aneurysmal trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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