Patient-reported outcome registry for spinal conditions and neuromodulation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, longitudinal observational registry that collects standardized patient-reported outcome measures and categorical diagnostic and treatment data at predefined follow-up moments for adults treated for spinal pathologies. It captures non-invasive treatments (for example injections and physical therapy), invasive procedures (for example surgery and radiofrequency therapies), and neuromodulation therapies such as spinal cord and DRG stimulation. The program aims to build large-scale outcome data, map patient flow through treatment modalities, and create patient profiles to guide personalized treatment strategies. Data will be collected at Jessa Hospital in Hasselt and shared for publication to inform care pathways and long-term response patterns.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Clinical diagnosis of spinal disease
2. Clinical indication to perform treatment of this disease
3. willing and capable to provide informed consent
4. Age ≥18 y

Exclusion Criteria:

not able to provide consent

Where it's running

• JEssa Ziekenhuis
  Hasselt, Limburg, Belgium Recruiting

Study contacts

• Study coordinator: Mark Plazier, M.D. PhD.
• Email: mark.plazier@jessazh.be
• Phone: +3211309071

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.