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RecruitingNCT06582810

Lidocaine Infusion Treatment for Subarachnoid Hemorrhage Headaches

Lidocaine Infusion As A Treatment Modality For Headache Following Non-Traumatic Subarachnoid Hemorrhage: A Prospective, Single-Center, Observational Cohort Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
University of Kansas Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Timeline

Start date
2025-01-31
Primary completion
2027-10-01
Completion
2028-07-01
First posted
2024-09-03
Last updated
2025-07-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06582810. Inclusion in this directory is not an endorsement.

Lidocaine Infusion Treatment for Subarachnoid Hemorrhage Headaches (NCT06582810) · Clinical Trials Directory