A Real-World Evidence Study to Evaluate the Effects of Voltaren Use on Mobility and Quality of Life in Participants With Knee Osteoarthritis Pain

Completed · Phase 4

Conditions studied: Pain

In brief

The purpose of this study is to investigate how topical diclofenac use can improve functional mobility and physical activity primarily, as well as other quality-of-life (QoL) parameters such as sleep, mood, and engagement in daily activities in participants with knee OA.

Key facts

Study ID

NCT06379893

Run by

HALEON

People needed

196

Starts

2024-04-25

Expected to finish

2024-10-29

Last updated by the study team

2026-01-20

Who can join

Age: 40 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant provision of a signed and dated informed consent document indicating that the participant has been informed of all pertinent aspects of the study before any assessment is performed.
• Participant is male or female who, at the time of screening, is between the ages of 40 and 85 years, inclusive.
• A participant who is willing and able to comply with scheduled visits, on-label Voltaren Gel use plan, and other study procedures.
• A participant willing to wear Actigraph continuously 24/7 for the study period.
• A participant in good general and mental health.
• A participant with diagnosed knee mild/non-serious osteoarthritis, proven via radiological evidence collected within the last 3 years.
• A participant with self-reported knee pain, with a score of greater than or equal to (>=) 40 millimeters (mm) less than or equal to (<=)70mm on the pain intensity visual analogue scale at the time of Informed Consent Form (ICF) signature.
• A participant willing to use Voltaren Gel for up to 3 weeks.

You may not qualify if…

• A participant who is an employee of the investigational site, either directly involved in the conduct of the study or a member of their immediate family; or an employee of the investigational site otherwise supervised by the investigator; or a Haleon employee directly involved in the conduct of the study or a member of their immediate family.
• A participant who has participated in other studies (including non-medicinal studies) involving investigational product(s) within 1 month prior to study entry and/or during study participation.
• A participant with, in the opinion of the investigator or medically qualified designee, an acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator or medically qualified designee, would make the participant inappropriate for entry into this study.
• A participant with confirmed rheumatologic disease
• A participant who has experienced trauma to the knee within the last 2 months that resulted in pain and/or swelling.
• A participant that has been administered local steroids or other Non-steroidal anti-inflammatory drugs (NSAIDs) injections to the knee within the last 3 months.
• A participant with recent history of major knee injury or surgery.
• A participant with knee skin area pathological condition which prevents application of product to the skins. Conditions such as: open skin wounds, infections, inflammations, or exfoliative dermatitis conditions.
• A participant with conditions not limited to the following: Gastrointestinal diseases, asthma, hypertension, myocardial infarction, thrombotic events, stroke, congestive heart failure, impaired renal function, or liver disease as judged by investigator or Site Staff.
• A participant diagnosed with other relevant medical conditions (example, psychiatric, neurological).
• A participant who takes medication relating to above conditions, such as tricyclic antidepressants or anticonvulsants.
• A participant with an active infection.
• A participant who is pregnant, lactating, or plan to be pregnant or lactating during the study.
• A participant with use of aspirin, Oral NSAIDs, topical treatment with any NSAIDs, warfarin, Angiotensin-converting enzyme (ACE) inhibitors, cyclosporine, diuretics, lithium or methotrexate, corticosteroids, or other anticoagulant therapy within 30 days of study.
• A participant with known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients, including hypersensitivity to NSAIDs and aspirin triad.
• A participant with any other acute or chronic illness that could compromise the integrity of study data or place the participant at risk by participating in the study.
• A participant who, in the opinion of the investigator or medically qualified designee, should not participate in the study.

Where it is running

• Tandem Clinical Research — Marrero, Louisiana, United States
• Quality Research Inc — San Antonio, Texas, United States
• Vitamed Gałaj I Cichomski sp.j. — Bydgoszcz, Poland
• Centrum Medyczne Lukamed. — Chojnice, Poland
• Silmedic sp. z o.o. — Katowice, Poland
• Santa Sp. z o.o. Santa Familia PTG Lodz — Lodz, Poland
• Centrum Badawcze Panaceum Agnieszka Brzezicka, Magdalena Lenkiewicz Sp z .o.o — Malbork, Poland
• Specjalistyczny Osrodek Lecziczo Badawczy (SOLB) Zbgniew Żęgota — Ostróda, Poland

Full record on ClinicalTrials.gov

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