Use of Synvisc® in Knee Osteoarthritis - Survey on Practice

N/ACompletedNCT02195544

Boehringer Ingelheim70 enrolled

Overview

Study of prescription methods in everyday medical practice, tolerance profile and effect of Synvisc® until six months of follow-up.

Study Type

OBSERVATIONAL

Enrollment

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * not applicable Exclusion Criteria: * none

Change in clinical symptoms

assessed via questionnaire

Time frame: up to 6 months

Amount of medication consumed

Time frame: up to 6 months

Patient satisfaction on a 4-point verbal rating scale

Time frame: up to 6 months

Number of patients with adverse events

Time frame: up to 6 months

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