Tracking outcomes of intravenous lidocaine for chronic pain

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study collects data on the performance and function of intravenous lidocaine infusions in adults with chronic pain. Participants are adults 18-80 who are scheduled to receive an IV lidocaine treatment for their condition. Data will be gathered to understand real-world outcomes and any safety signals associated with this therapy in a clinical setting. The study is sponsored by the International Spine, Pain and Performance Center and conducted at their Washington D.C. location, without a formal intervention beyond the planned infusion.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age 18-80 years
* Patients with chronic pain syndrome
* Patients that have been prescribed and scheduled to receive an intravenous lidocaine infusion treatment

Exclusion Criteria:

* Not willing to comply with the requirements of the study

Where it's running

• International Spine Pain & Performance Center
  Washington D.C., District of Columbia, United States Recruiting

Study contacts

• Study coordinator: Victoria Brownlee, MPH
• Email: vbrownlee@isppcenter.com
• Phone: 202-849-8333

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.