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COMPLETED
NCT01536314
PHASE3

Prophylaxis of Neuropathic Pain by mémantine

Sponsor: University Hospital, Clermont-Ferrand

View on ClinicalTrials.gov

Summary

The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.

Official title: Preventing the Development of Neuropathic Pain Post-mastectomy/Tumorectomy by Pre-emptive or Post-operative Memantine Administration

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

43

Start Date

2012-02

Completion Date

2013-11

Last Updated

2026-08-05

Healthy Volunteers

No

Interventions

DRUG

Memantine EBIXA®

The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.

DRUG

Placebo : lactose

The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.

Locations (1)

CHU Clermont-Ferrand

Clermont-Ferrand, France