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NCT01121653

Impact of Oral Magnesium on Neuropathic Pain

Completed Phase 4 Last updated 10 May 2010
What this trial tests

Phase 4 trial testing Magnogene ® (magnesium) in Patient With Neuropathic Pain in 50 participants. Completed in 1 June 2008.

Timeline
1 March 2006
Primary endpoint
1 January 2008
1 June 2008

Quick facts

Lead sponsorUniversity Hospital, Clermont-Ferrand
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Maskingdouble
Primary purposetreatment
Enrollment50
Start date1 March 2006
Primary completion1 January 2008
Estimated completion1 June 2008
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Clermont-Ferrand

Who can join

18 and older, any sex, with Patient With Neuropathic Pain. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

Use lay language. The aim of this study is to evaluate on pain scores (neuropathic pain questionnaire and pain numeric scale) and on quality of life, the effect of oral magnesium intake on patients with neuropathic pain comparing with patients receiving placebo,. The study drug will be taken during 4 weeks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other University Hospital, Clermont-Ferrand trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing