Exploring the Benefit of Topical Capsaicin in Treating Pain From Chemo-induced Peripheral Neuropathy: a Longitudinal Single Center Pilot Study

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

To learn if topical capsaicin can help relieve pain from CIPN and improve gait (the pattern of walking) in patients.

Eligibility criteria

Qualifiers

Participants diagnosed with pain of the lower extremity from chronic (>90 days duration) CIPN (due to either vinca alkaloids, taxanes, bortezomib, thalidomide, platinum-based compounds), seen at MD Anderson Cancer Center

Participants reporting baseline pain ≥ 4 (0-10 scale, NRS)

Participants age 18+

Participants who have completed chemotherapy within the last year at the time of enrollment.

Disqualifiers

Participants with cognitive dysfunction

Participants with recent history (<6 months) of drug or alcohol abuse

Participants with open skin lesion or undergoing antibiotic therapy for local for systemic infection

Participants with allergies to capsaicin or adhesives

Trial design

Treatments tested in this trial

  • Qutenza Patch

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

M.D. Anderson Cancer Center

Lead sponsor

Averitas Pharma, Inc.

Collaborator