A Phase 3 Study to Evaluate the Long-Term Safety of ThermoProfen™ in Patients With Mild to Moderate Pain Associated With Osteoarthritis of the Knee.
Public ClinicalTrials.gov record NCT00532038. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
An Open-Label, Long-Term Safety Study to Evaluate the Safety of ThermoProfen™ for the Treatment of Mild to Moderate Pain Associated With Osteoarthritis of the Knee
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
ThermoProfen is a transdermal ketoprofen patch that is integrated with a long-lasting CHADD (Controlled Heat-Assisted Drug Delivery) unit for the treatment of chronic pain associated with osteoarthritis. This study will evaluate the safety of long-term administration of ThermoProfen™ for the pain associated with osteoarthritis of the knee in adults. The study will be conducted in patients with pain associated with osteoarthritis and who have completed a previous efficacy study of ThermoProfen.
Study identification
- NCT ID
- NCT00532038
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 179 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 18 Years to 75 Years
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 31, 2007
- Primary completion
- Oct 31, 2008
- Completion
- Oct 31, 2008
- Last update posted
- Mar 15, 2012
2007 – 2008
United States locations
- U.S. sites
- 20
- U.S. states
- 14
- U.S. cities
- 20
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Not listed | Anaheim | California | 92801 | — |
| Not listed | San Diego | California | 92103 | — |
| Not listed | Westlake Village | California | 91361 | — |
| Not listed | Clearwater | Florida | 33761 | — |
| Not listed | Pembroke Pines | Florida | 33024 | — |
| Not listed | Springfield | Illinois | 62704 | — |
| Not listed | Evansville | Indiana | 47714 | — |
| Not listed | Overland Park | Kansas | 66215 | — |
| Not listed | Baltimore | Maryland | 21239 | — |
| Not listed | Wheaton | Maryland | 20902 | — |
| Not listed | Kansas City | Missouri | 64114 | — |
| Not listed | Mercerville | New Jersey | — | — |
| Not listed | Raleigh | North Carolina | 27612 | — |
| Not listed | Lake Oswego | Oregon | 97035 | — |
| Not listed | Duncansville | Pennsylvania | 16635 | — |
| Not listed | Erie | Pennsylvania | 16508 | — |
| Not listed | Anderson | South Carolina | 29621 | — |
| Not listed | Nashville | Tennessee | 37205 | — |
| Not listed | Houston | Texas | 77090 | — |
| Not listed | San Antonio | Texas | 78217 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
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About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00532038, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Mar 15, 2012 · Synced Sep 1, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00532038 live on ClinicalTrials.gov.