Can tracking daily life with knee osteoarthritis improve care?
NCT ID NCT06623773
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This study follows 136 adults aged 50 to 85 with knee osteoarthritis who are taking the supplement Structum (chondroitin sulfate). Researchers will measure pain, stiffness, and physical function using a standard questionnaire, along with other health factors, at the start and after three months. The goal is to describe the real-world burden of the disease and how it affects quality of life in Poland. Since this is an observational study, it does not test whether Structum works, but rather paints a picture of patients' experiences.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Chondroitin sulfate (Structum), a natural supplement-like drug for osteoarthritis symptoms
- What this could lead to
- If successful, this study could clarify how much knee osteoarthritis affects daily life and whether current treatment patterns match patients' needs, possibly guiding better care strategies.
- What could go wrong
- This is an observational study without a control group, so it cannot prove whether Structum works. Results may not apply beyond the Polish population studied.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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136 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Oct 2024
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population will include adult patients aged 50 to 85 years with a confirmed diagnosis of knee osteoarthritis and a new prescription for Structum®, as treated by participating centers in Poland.
- Ages
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50 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female patients aged 50 to 85 years at inclusion * of knee OA (either a patient newly diagnosed \[at inclusion\] or with history of knee OA) based on at least the following items 1 and/or 2: 1. knee pain lasting for at least 3 months; 2. patient in the active phase of knee OA disease (knee pain score ≥ 40mm at inclusion on the Visual Analog Scale \[VAS\] 0-100 mm); 3. knee radiographs showing knee joint narrowing and/or osteophytes. * Patients who have been prescribed, for the first time or not, Structum®. * patient taking any non-steroidal anti-inflammatory drugs (NSAIDs) or other analgesics should be on stable dose at least one week before inclusion to the study. * Patients able to visit the clinic and attend follow-up visits. * Patients having signed an informed consent form, according to local regulations. Exclusion Criteria: * Patients with any ongoing chondroitin sulfate treatment at inclusion or during the last 3 months. * plasma (in the last 3 months). No glucocorticoids administration in the last 3 months before inclusion. That does not include NSAIDS, paracetamol and other analgesic medications (e.g. tramadol). * Patients with an artificial knee joint, including unilateral. * Patients scheduled to undergo knee replacement surgery in the next 6 months. * Patients with a severe general condition that prevents them from being included in the study as assessed by the investigator. * Patients participating in interventional trials on investigational drugs at the time of inclusion.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Agnieska WIAK
Lubartów, 21-100, Poland
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Alina Wołkowicz Mruk
Krakow, 31-455, Poland
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Andrzej Majer
Kujakowice Gorn, 46-211, Poland
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Bartlomiej Szpyra
Krakow, 31-155, Poland
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Elżbieta Pietrus- Dunaszewska
Katowice, 40-007, Poland
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Maciej Dołżyński
Bialystok, 15-481, Poland
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Marcin Milchert
Szczecin, 71-497, Poland
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Mariusz Borowiecki
Zielona Góra, 65-559, Poland
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Michał Straburzyński
Zielona Góra, 65-047, Poland
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Piotr Ligocki
Bydgoszcz, 85-091, Poland
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Sławomir Panek
Olesno, 46-300, Poland
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Viktor Kostiuk
Żagań, 68-100, Poland
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Wojciech Larczyński
Nowy Dwór Gdański, 82-100, Poland
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Wojciech Roczniak
Ustrzyki Dolne, Ustrzyki Dolne, Poland
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Zdzisław Derleta
Warsaw, 03-938, Poland
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Other studies related to the condition(s) this trial covers.
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