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Drug Use Survey (DUS) of Triple Therapy (Methycobal (MBL)+ Myonal (MYO)+ Non-steroidal Anti-inflammatory Drags (NSAID)) on the Symptom Relief of Lumbar DDD in China

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Eisai

Status

Completed

Conditions

Lumbar Disc Degenerative Disease

Study type

Observational

Funder types

Industry

Identifiers

NCT01299077
EISAI-MBL-2010-1

Details and patient eligibility

About

The purpose of this study is to observe the overall satisfaction of patients with degenerative disc disease after receiving triple therapy.

Full description

DDD (lumbar disc degenerative disease ) patients who have been prescribed triple therapy (MBL+ MYO+ NSAIDs) over 2 weeks of triple therapy were enrolled in the study. They were asked to assess their overall satisfaction degree on triple therapy.

Enrollment

478 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. lumbar degenerative disc disease (DDD)
  2. patients who have been prescribed over 2 weeks of triple therapy

Exclusion criteria

Patients who do not meet inclusion criteria for DDD

Trial design

478 participants in 1 patient group

Lumbar disc degenerative disease
Description:
Triple therapy (MBL+ MYO+ NSAIDs) which prescribed by doctors (Drs) based on disease condition

Trial contacts and locations

10

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Data sourced from clinicaltrials.gov

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