Skip to content

Injectable Cold Energy Therapy For The Management Of Chronic Pain Associated With Osteoarthritis Of The Knee

Active, not recruitingNot applicableNCT06700109
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The goal of this clinical trial is to evaluate the effectiveness of Neural Ice for pain management associated with knee osteoarthritis in adults aged 22-80 years. Participants will attend study visits and complete subject diaries. Participants will be followed for 6 months after study procedure.

Study details

Official title
Injectable Cold Energy Therapy For The Management Of Chronic Pain Associated With Osteoarthritis Of The Knee: A Multi-Center, Randomized, Controlled Study (Ice Study)
Conditions
  • Osteoarthritis (OA) of the Knee
Interventions
  • Device: Neural Ice
  • Drug: Triamcinolone acetate
Sponsor
Brixton Biosciences, Inc.
Start date
2024-11-19
Primary completion
2027-02-01
Sex
All
Age range
from 22 Years to 80 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
15

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Age 22 to 80, inclusive of any gender 2. Baseline pain intensity of \>/= 5 of the Numeric Rating Scale (NRS) despite current treatment Confidential Brixton Biosciences Inc. Page 12 of 53 Version: 1.1, 30 August 2024 3. Chronic symptomatic osteoarthritis of the knee (K-L stage 2, 3, or 4) on plain x-rays obtained within the previous 12 months 4. At least 3 months of previous conservative treatments (NSAID, acetaminophen, physical therapy, cortisone injections) that are not currently providing relief 5. Agree to see one doctor (study investigator) for knee pain during the study period 6. Willing/able to understand the informed consent form and provide written informed consent 7. Able to complete outcome measures (including electronic patient reported outcome measures) Exclusion Criteria: 1. Known allergy to glycerol, hyaluronic acid, poloxamer 407, or phosphate buffered saline 2. History of cryoglobulinemia 3. History of cold-induced auto-immune hemolytic anemia (e.g. paroxysmal cold hemoglobinuria or cold agglutinin disease) 4. History of cold urticaria 5. History of Chilblain's (pernio) disease in the lower extremities 6. History of Raynaud's disease 7. Open and/or infected wounds or active tumor at or near the treatment site 8. History of vascular surgery involving femoral vessels on the injection side 9. History of surgical procedures to affected limb that, in the opinion of the investigator, could have impacted the integrity of the genicular nerves or blood vessels 10. Active bacterial or fungal infection that at the discretion of the investigator would preclude study participation 11. Currently taking \>60 MME/day, as determined per MDcalc.com (opioid conversion calculator) 12. History of History of systemic inflammatory conditions such as rheumatoid arthritis 13. Bleeding disorders anticoagulant therapy, unless appropriately stopped or reversed for the procedure 14. Any condition or circumstance that would impact or confound assessment of safety and/or pain. For example, comorbid or concomitant pain conditions, pre-existing lower limb neurologic deficits, any psychiatric or neurologic disease 15. Cryoneurolysis, thermal or pulsed radiofrequency ablation, or phenol injection for the index knee within the past 12 months 16. Use of intra-articular injection of corticosteroid within the previous 3 months, or hyaluronic acid, prolotherapy, Confidential Brixton Biosciences Inc. Page 13 of 53 Version: 1.1, 30 August 2024 autologous blo…

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06700109