NCT Number: NCT02195557
Retrospective Follow-up Study of Synvisc® in Patients With Knee Osteoarthritis
Retrospective collection of data, aimed at a better knowledge of the use of Synvisc® among the patients with knee osteoarthritis (OA) since at least three years.
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Notify MeKey information
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients with knee osteoarthritis using Synvisc® since at least three years
Exclusion criteria
- none
Treatment and study plan
Primary outcomes
-
Reason for prescription
Time frame: at least 3 years before start of observation period
-
Number of other treatments per patient
Time frame: at least 3 years of observation
antalgics, non-steroid anti-inflammatory drugs (NSAIDs), steroid anti-inflammatory drugs (SAIDs), specific symptomatic treatments and surgery
-
Time between two treatments
Time frame: at least 3 years of observation
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Official study title
Synvisc® in Knee Osteoarthritis: Retrospective Follow-up in Treated Patients Since at Least Three Years
Important dates
- Study start
- 2002
- Primary completion
- 2003
- First posted
- Jul 21, 2014
- Registry last updated
- Jul 22, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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