Outpatient Midline Catheter in Patients Receiveing Lidocaine Infusion Series.

Sponsor
Medical University of Warsaw
Study ID
NCT07555314
Status
Recruiting
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Conditions

  • Chronic Pain
  • Lidocaine Infusion
  • Midline Catheter
  • Outpatient

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

This study will assess the efficacy, safety and practicality of using midline catheters for repeated intravenous lidocaine infusions in an outpatient pain management setting. Adult patients requiring serial lidocaine infusions for chronic pain will be enrolled and receive treatment through midline catheters over ten sessions. The study will investigate if the midline catheters are a safe and effective option for delivering repeated lidocaine infusions in the outpatient setting, offering a balance between ease of placement, acceptable complication risk and good patients' comfort.

Key Dates

First listed
Apr 29, 2026
Start date
Apr 20, 2026
Status verified
Apr 2026
Primary completion
Dec 30, 2027
Completion
Jun 1, 2028

Study Design

Enrollment
500 participants (estimated)

Arms

  • Arm: Outpatient midline catheter
    Patients who receive a midline catheter for lidocaine infusion daily for ten days with two days weekend pause.

Primary Outcome Measure

Successful lidocaine infusion therapy without the need for additional venous access [ Time Frame: 12 days (from midline insertion to the end of the therapy) ]

Central Contacts

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