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Examination of Vertebroplasty in Addition to Regular Treatment of Patients With Multiple Myeloma.

Key facts

Where
Middelfart, DániaSee the site

Where in Dánia

  • Center for Spine Surgery and ResearchMiddelfart, DániaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Spine Centre of Southern Denmark
Trial code
NCT04533217
Record updated
2024. december 3.
Original description
Patients with newly diagnosed or known multiple myeloma with newly diagnosed vertebral lesion(s) will be invited to participate in a cross-sectoral randomized controlled trial. The trial will compare two groups of patients which either receive regular medical treatment of their vertebral lesion(s) or vertebroplasty in addition to regular medical treatment. Our goal is to investigate the effectiveness of vertebroplasty and determine the role of surgical treatment in the overall treatment of patients with multiple myeloma and vertebral lesion(s).Read full original descriptionShow less

Palliative Treatment of Patients With Multiple Myeloma and Painful Vertebral Lesions. A Cross-sectoral Randomized Controlled Trial of Vertebroplasty in Addition to Regular Medical Treatment.

Patients with newly diagnosed or known multiple myeloma with newly diagnosed vertebral lesion(s) will be invited to participate in a cross-sectoral randomized controlled trial. The trial will compare two groups of patients which either receive regular medical treatment of their vertebral lesion(s) or vertebroplasty in addition to regular medical treatment. Our goal is to investigate the effectiveness of vertebroplasty and determine the role of surgical treatment in the overall treatment of patients with multiple myeloma and vertebral lesion(s).

Inclusion: known multiple myeloma; verified lesion(s) between Th6-L5; 4 or less fractures; relevant pain in 3 months or less; vertebroplasty can be performed in one procedure; VAS 5 or more.

Exclusion: psychological or psychiatric disorder hat is expected to interfere with compliance; presence of neurologic deficit.

ClinicalTrials.gov NCT04533217