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Effects of Osteopathic Management on Disability and Quality of Life After Lumbar Arthrodesis

RecruitingNAAges 18 Years - 75 YearsAllClinique Bizet
NCT06802120 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The aim of our study is to assess the effect of a combined physiotherapy and osteopathy treatment versus a placebo on the management of disability and quality of life after lumbar arthrodesis. This study will provide a better assessment of the use of osteopathy as a non pharmacological approach to post-operative management. For this purpose, We will analyze the effects of these two approaches, targeted and non-targeted osteopathy (TO vs. NTO), on patients' disability and quality of life after surgery.

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📋 Eligibility rules (as published)
Inclusion Criteria: * having experienced a lumbar arthrodesis (of one to three levels) four weeks before inclusion * being under a stable pharmacological treatment over the last month * who are suffering from postoperative mechanical pain (VAS ≥ 4) Exclusion Criteria: * neuropathic pain according to a DN4 score greater than or equal to 4/10, * are suffering from fibromyalgia, * algodystrophy, * other somatic or neuropsychiatric diseases (other than depression and anxiety), * have received osteopathic treatment over the last three month prior to inclusion, * are included in another interventional research protocol during the study period
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What it tests

  • osteopathy real
  • sham osteopathy
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Where

1 site
Clinique Bizet
Paris, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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