Trials / Unknown
UnknownNCT01264237
Evaluation of the Efficacy, Tolerability and Safety of Etoricoxib (Arcoxia) in Patients With Neuropathic Pain
An Enriched Enrollment, Double-Blind, Placebo-Controlled, Parallel Group, Randomized Withdrawal Trial to Evaluate the Efficacy, Tolerability and Safety of Etoricoxib (Arcoxia) in Patients With Moderate to Severe Neuropathic Pain
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- Sponsor
- Analgesic Solutions · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The present study will aim to determine the safety, efficacy, and tolerability of etoricoxib, an NSAID pain reliever, in patients with Neuropathic pain. Neuropathic pain, or pain caused by abnormal activity of sensory neurons, remains undertreated. Post herpetic neuralgia (PHN), which is commonly referred to as post-shingles pain, is the most useful disease to study when investigating the efficacy of pain relievers for Neuropathic pain. Therefore, this study will primarily involve patients with PHN. The hypothesis in this study is that etoricoxib efficacy is superior to that of placebo.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Etoricoxib | 90mg Tablet QD at 10:00a.m. |
| DRUG | Placebo | One tablet QD at 10:00a.m. |
Timeline
- Start date
- 2011-03-01
- Primary completion
- 2011-08-01
- Completion
- 2012-04-01
- First posted
- 2010-12-21
- Last updated
- 2011-03-23
Locations
2 sites across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT01264237. Inclusion in this directory is not an endorsement.