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OpenTrials
Completed

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.

Completed

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Key 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

Synvisc®

Drug

Primary outcomes

  1. Reason for prescription

    Time frame: at least 3 years before start of observation period

  2. 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

  3. 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.

Published trials that share one or more normalized conditions with this study.