WHO ICTRP trial
A randomised, double-blind, placebo (vehicle) controlled, parallel group study…
EUCTR2008-002655-24-DK · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2008-002655-24-DK |
|---|---|
| Public title | A randomised, double-blind, placebo (vehicle) controlled, parallel group 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. |
| Scientific title | A randomised, double-blind, placebo (vehicle) controlled, parallel group 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. |
| Primary sponsor | SantoSolve A/S |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Countries | Germany;United Kingdom;Denmark |
| Conditions | Post amputation patients (at least 6 months prior to visit 1) with chronic moderate-to-severe lower limb stump pain, defined as average stump pain on a daily basis (=40 on a 100 mm pain VAS scale) despite proper healing of the wound… |
| Interventions | Product Name: 2PX Product Code: 2PX Pharmaceutical Form: Cutaneous solution INN or Proposed INN: strontium chloride hexahydrate Current Sponsor code: 2PX Other descriptive name: 2PX Concentration unit: % (W/V) percent weight/volume… |
| Registration date | Aug 29, 2008 |
| Target size | 150 |
| Secondary IDs | SMR-1850/2PX-SP-02 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: