Osteoarthritis Trial, Recruiting NCT05407610 Sponsor: Ziekenhuis Oost-Limburg Condition: Osteoarthritis
Back to Osteoarthritis

Osteoarthritis Trial, Recruiting

NCT05407610
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 or older.
  • People who have had ongoing front-of-knee pain for more than 12 months that is moderate to severe (a pain score above 4 out of 10 on most or all days, either all the time or when moving).
  • People whose knee pain has not been adequately relieved — or who could not tolerate — at least 12 months of conventional treatments, which must have included all three of the following: active physiotherapy, pain medications, and steroid injections into the knee joint.
  • People with knee osteoarthritis (OA): imaging taken within the past 12 months must confirm a mild, moderate, or severe grade of OA in the affected knee, as assessed by an independent specialist radiologist.
  • People with ongoing pain after a total knee replacement surgery (also called Total Knee Arthroplasty): an orthopaedic review must have ruled out surgical or structural causes for the continued pain.
  • People who are willing and able to sign a consent form before any study assessments begin.

Who may not be able to join:

  • People with an active local or widespread infection, including infection in the bloodstream.
  • People whose knee pain is caused by inflammatory arthritis or another inflammatory condition affecting the whole body.
  • People who have had any injection into the affected knee (such as steroids, hyaluronic acid, or platelet-rich plasma) in the three months before the procedure.
  • People who are pregnant, breastfeeding, or planning to become pregnant before the study treatment is given.
  • People who experience widespread chronic pain across their body (not just the knee).
  • People with an unstable psychological or psychiatric condition.
  • People with a known allergy to any of the substances used during the procedure, including lidocaine, propofol, or chlorhexidine.
  • People with poorly controlled blood clotting problems, defined as taking a higher-than-prescribed dose of blood-thinning medication.
  • People with poorly controlled immune suppression.
  • People who have participated in another clinical trial within the 30 days before signing the consent form.
  • People who currently have a nerve stimulator device implanted in their body.
  • People who currently have shooting or radiating pain travelling down the leg on the same side as the affected knee.
  • People who have previously had a radiofrequency treatment (standard or cooled) on the affected knee.
  • People who have moderate to severe chronic pain in both knees (pain above 4 out of 10 on most or all days for more than 12 months in both knees) that has not responded to at least 12 months of conventional treatments including physiotherapy, pain medications, and steroid injections.
  • People who already have a confirmed date scheduled for a total knee replacement surgery.
  • People who are unwilling or unable to complete the study questionnaires.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 14 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +32 (0)89 32.52.54

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Ziekenhuis Oost-Limburg
Registry
ClinicalTrials.gov
Start date
7 July 2022
Est. completion
1 March 2025

Where this trial is recruiting

🇧🇪 Belgium 🇳🇱 Netherlands

Primary endpoints

The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) at 6 months post-intervention

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov