Clinical Trial

Periganglionic Resiniferatoxin for the Treatment of Intractable Pain Due to Cancer-induced Bone Pain

Not Yet Recruiting Phase 1/2
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Summary
Background: Cancer-induced bone pain (CIBP) is common in people with cancer. Bone cancer can also lead to anxiety, depression, and reduced mobility and quality of life. Researchers believe a research drug called resiniferatoxin (RTX) may be able to help. Objective: To learn whether RTX is safe and can reduce cancer induced bone pain. Eligibility: People ages 18 and older with CIBP that is not relieved by standard treatments Design: Participants will have up to 6 outpatient visits over about 7 months. These will include: Medical history Physical exam Blood and urine tests. Thermal testing: a disk placed on the skin to test ability to sense temperature in and around the area of pain Chest x-ray EKG: stickers are placed on the chest to measure heart signals ECG: measures electrical activity of the heart Participants will have 1 inpatient visit lasting 2-4 days. This will include: Catheter inserted into a vein in the arm. They are given anesthesia, sedation, and x-ray contrast. A needle is passed through the skin of the back to inject the RTX. Participants will keep a log of the pain medications they take after surgery. Participants will be called 1 week and 2, 3, and 4 months after the injection. Participants will be mailed surveys and questionnaires to complete 2, 3, and 4 months after the injection. ...
Protocol Amendment History 306 amendments
This ClinicalTrials.gov record has been amended 306 times since 2015-08-12; most recent amendment 2026-06-13.
Status change: Recruiting → Not Yet Recruiting 2020-03-18
Status change: Not Yet Recruiting → Recruiting 2020-01-17
Status change: Suspended → Not Yet Recruiting 2019-11-26
Status change: Recruiting → Suspended 2019-04-27
Status change: Suspended → Recruiting 2018-08-28
Trial Details
NCT Number NCT02522611
Lead Sponsor National Institute of Neurological Disorders and Stroke (NINDS)
Conditions Intractable Pain, Palliative Care
Enrollment 30 participants
Start Date 2026-08-27
Primary Completion 2026-12-01 (estimated)
Study Completion 2026-12-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-07