NCT00452010View on ClinicalTrials.gov

Pain Reducing Effect of Transcutaneous Electrical Nerve Stimulation in Patients With Chronic Low Back Pain or Lumbo-radiculalgia

PHASE4CompletedINTERVENTIONAL
Enrollment

236

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

September 30, 2008

Study Completion Date

September 30, 2008

Conditions
Chronic Low Back PainChronic Lumbo-radiculalgia
Interventions
DEVICE

CEFAR PRIMO TENS Class IIA (active)

Active TENS. 4 sessions per day during 3 months.

DEVICE

CEFAR PRIMO TENS Class IIA (no active)

Placebo TENS. 4 sessions per day during 3 months.

Trial Locations (8)

13000

Fondation Hôpital Saint Joseph - MARSEILLE, Marseille

La Timone - MARSEILLE, Marseille

38000

CHU de Grenoble, Grenoble

38500

CH de Voiron, Voiron

42055

CHU de Saint-Etienne, Saint-Etienne

44000

Centre Catherine de Sienne - Nantes, Nantes

80000

CHU d'Amiens, Amiens

87000

CHU de Limoges, Limoges

All Listed Sponsors
collaborator

Ministry of Health, France

OTHER_GOV

lead

Centre Hospitalier Universitaire de Saint Etienne

OTHER

NCT00452010 - Pain Reducing Effect of Transcutaneous Electrical Nerve Stimulation in Patients With Chronic Low Back Pain or Lumbo-radiculalgia | Biotech Hunter | Biotech Hunter