Trials / Unknown
UnknownNCT00804375
Study of the Efficacy, Safety and Tolerability of Topical 2PX (Strontium Chloride Hexahydrate) in Patients With Chronic, Moderate-to-severe Lower Limb Post-amputation Stump Pain
Study of the Efficacy, Safety and Tolerability of Topical 2PX (Strontium Chloride Hexahydrate) in Patients With Chronic, Moderate-to-severe Lower Limb Post-amputation Stump Pain.
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- Sponsor
- Smerud Medical Research International AS · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Primary: To compare the analgesic effect over 12 weeks of topical 2PX in stump pain. Secondary: To prospectively measure other efficacy and safety variables of topical 2PX in stump pain. Exploratory analyses will be performed to measure efficacy and safety variables of topical 2PX in phantom pain
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | 2PX | cutaneous solution to be applied twice daily for 84 days |
| DRUG | Placebo | cutaneous solution to be applied twice daily for 84 days |
Timeline
- Start date
- 2008-12-01
- Primary completion
- 2010-06-01
- Completion
- 2010-06-01
- First posted
- 2008-12-08
- Last updated
- 2010-03-24
Locations
19 sites across 5 countries: Denmark, Germany, Norway, Russia, United Kingdom
Source: ClinicalTrials.gov record NCT00804375. Inclusion in this directory is not an endorsement.