New gel shot for hip pain: could it replace surgery?
NCT ID NCT07232199
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a gel called Sensovisc, made of sodium hyaluronate, injected into the hip joint to relieve pain from osteoarthritis. The gel aims to restore the joint's natural fluid, reducing pain and improving movement. Researchers will track 25 adults with moderate hip arthritis over 6 months to see if the gel safely eases pain during rest, activity, and sleep.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sodium hyaluronate gel (Sensovisc)
- What this could lead to
- If it works, this could offer a non-surgical option to reduce hip pain and improve joint function for people with osteoarthritis.
- What could go wrong
- This is a very small, early study with only 25 people. It may not show clear benefits, and results may not apply to everyone with hip arthritis.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2025
An estimate. Start dates often move.
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- 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: * \>18 years old * Patients who have unilateral and/or bilateral hip pain for more than 3 months and meet the diagnosis of coxarthrosis according to ACR criteria * 40 mm above the pain level determined by the Visual Analogue Scale (VAS) during rest for at least 15 days in the month before starting the study (for paracetamol and oral NSAIDs, taking into account the half-life of the drug). * Diagnosis of hip osteoarthritis with Stage II or III according to the Kellgren and Lawrence (KL) classification, as determined by x-rays taken in the last 12 months * Ambulating with or without support * Having the mental ability to express pain scores * Signing the informed consent form indicating consent to participate in the study Exclusion Criteria: * Radiological Kellgren-Lawrence (K\&L) stage I or IV * Other non-degenerative causes of hip pain * septic arthritis * Avascular necrosis, * Femoroacetabular impingement syndrome, * Trochanteric bursitis * Having a history of lower extremity fracture/surgery within the last 6 months * Pregnancy, breastfeeding, pregnancy plan * Morbidly obese patients (BMI\>40), * Patients with unstable medical conditions (liver or kidney failure, lung/heart disease, tumor, HIV, etc.) * Known central nervous system and/or peripheral nervous system disease * When fluoroscopy guided injection is contraindicated: * pregnancy, * contrast material allergy, * local anesthetic allergy, * Having conditions such as coagulopathy * Related to Treatment * Corticosteroid injection into the target joint within the last 1 month before the first injection * Hyaluronan injection into the target joint within the last 6 months before the first injection * Arthroscopy or surgery on the target joint within the last 6 months before the first injection * Those who use blood thinners (warfarin compounds and heparin) or have bleeding problems * Contraindications for SENSOVISC: Hypersensitivity to product ingredients, systemic infection, presence of local infection on the buttocks, infection or skin disease at the injection site or joint area
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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