London, United Kingdom
NCT Number: NCT02139319
Dose-Escalation of Botulinum Toxin in Subjects With Osteoarthritis of the Knee
The purpose of the study is to evaluate the safety and tolerability of the drug product at each dose level.
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Notify MeKey information
Conditions
Age range
25 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Osteoarthritis of the knee
- Fully weight bearing in the index knee with or without the need for assistive/orthopaedic devices
- Pain score ≥40 mm of the index knee
- Committing to continue using their assistive/orthopaedic device throughout the study using the same regimen
Exclusion criteria
- Any infection in the index knee or inflammatory skin disease or other inflammatory diseases at the index knee or the anticipated injection site
- Surgery on the symptomatic knee within the previous 12 months or arthroscopy in the index knee in the past 3 months
- Any painful orthopaedic disorder of the back or hip which is likely to interfere with the safety or efficacy assessments
- A joint disorder other than osteoarthritis in the index knee which could potentially interfere with the safety or efficacy assessments
Treatment and study plan
Botulinum toxin
DrugPlacebo
DrugPrimary outcomes
-
Incidence and severity of adverse events
Time frame: Up to 6 weeks
Sponsors and collaborators
Lead sponsor
Galderma R&D
Industry
Registry information
Important dates
- Study start
- 2014
- Primary completion
- 2014
- Study completion
- 2014
- First posted
- May 15, 2014
- Registry last updated
- Aug 25, 2022
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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