Lidocaine Infusion Treatment for Subarachnoid Hemorrhage Headaches
Recruiting now
Conditions studied: Subarachnoid; Hemorrhage, Nontraumatic, Headache
In brief
The goal of this observational study is to evaluate intravenous lidocaine efficacy and safety in treating headache following non-traumatic subarachnoid hemorrhage. Through this prospective analysis, the investigators hope to: 1. show that intravenous lidocaine infusion causes a clinically significant reduction in pain scores in patients with moderate/severe headache pain following non-traumatic subarachnoid hemorrhage; 2. show that intravenous lidocaine infusion is safe in treating headache following non-traumatic subarachnoid hemorrhage; 3. and report vasospasm prevalence in the cohort. Participants will receive lidocaine infusion as treatment for non-traumatic subarachnoid hemorrhage headache and provide pain scores (on a numeric pain scale) every two hours the patients are awake for a maximum of seven days. Monitoring for vasospasm will occur as part of the patients regular medical care.
Key facts
- Study ID
- NCT06582810
- Run by
- University of Kansas Medical Center
- People needed
- 20
- Starts
- 2025-01-31
- Expected to finish
- 2028-07-01
- Last updated by the study team
- 2026-07-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients > 18 years;
- Have a favorable neurological status defined as Hunt and Hess score ≤ 3 (as it accounts for patient awareness);
- Can communicate numeric pain scores;
- Are diagnosed with non-traumatic subarachnoid hemorrhage
You may not qualify if…
- The patient is diagnosed with traumatic subarachnoid hemorrhage;
- If the patient is < 18 years of age;
- If numeric pain scores could not be captured for > 3 days of hospitalization;
- If the patient had a prior aneurysm;
- Chronic pain not associated with non-traumatic subarachnoid hemorrhage diagnosis;
- A disability before the stroke (> 2 on modified Rankin Scale score);
- A Hunt and Hess score > 3;
- Contraindications to lidocaine (significant cardiac disease, arrhythmia, seizures, previous allergic reaction to lidocaine
Where it is running
- Ascension Via Christi St. Francis — Wichita, Kansas, United States (enrolling)
Full record on ClinicalTrials.gov
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