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Retrospective Follow-up Study of Synvisc® in Patients With Knee Osteoarthritis

Synvisc® in Knee Osteoarthritis: Retrospective Follow-up in Treated Patients Since at Least Three Years

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02195557
Enrollment
16
Registered
2014-07-21
Start date
2002-04-30
Completion date
Unknown
Last updated
2014-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis

Brief summary

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.

Interventions

Sponsors

Boehringer Ingelheim
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Patients with knee osteoarthritis using Synvisc® since at least three years

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Reason for prescriptionat least 3 years before start of observation period
Number of other treatments per patientat least 3 years of observationantalgics, non-steroid anti-inflammatory drugs (NSAIDs), steroid anti-inflammatory drugs (SAIDs), specific symptomatic treatments and surgery
Time between two treatmentsat least 3 years of observation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026