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NCT02195544 Clinical Trial

Use of Synvisc® in Knee Osteoarthritis - Survey on Practice

Osteoarthritis Clinical Trial

Official title:
Use of SYNVISC in Knee Osteoarthritis. Survey on Practice. "U.S.A.G.E Pratique"

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02195544
Other study ID # 1139.5
Secondary ID
Status Completed
Phase N/A
First received July 18, 2014
Last updated July 18, 2014
Start date October 1998

Study information
Verified date July 2014
Source Boehringer Ingelheim
Contact n/a
Is FDA regulated No
Health authority France: Conseil National de l'Ordre des Médecins
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date
Est. primary completion date April 2000
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Drug:
• Synvisc®

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Boehringer Ingelheim

Outcome
Type Measure Description Time frame Safety issue
Primary Change in clinical symptoms assessed via questionnaire up to 6 months No
Primary Amount of medication consumed up to 6 months Yes
Primary Patient satisfaction on a 4-point verbal rating scale up to 6 months No
Secondary Number of patients with adverse events up to 6 months No
See also
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