Assessing osteopathy's impact on recovery after back surgery
Effects of Osteopathic Management on Disability and Quality of Life After Lumbar Arthrodesis. A PARALLEL, RANDOMIZED AND DOUBLE-BLIND CONTROLLED PILOT STUDY
NA · Clinique Bizet · NCT06802120
This study tests if combining physiotherapy with osteopathy can help people recover better and feel more comfortable after back surgery compared to a placebo.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Clinique Bizet (other) |
| Locations | 1 site (Paris) |
| Trial ID | NCT06802120 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a combined physiotherapy and osteopathy treatment compared to a placebo in managing disability and improving quality of life for patients who have undergone lumbar arthrodesis. It focuses on analyzing the effects of targeted and non-targeted osteopathy on postoperative recovery. The goal is to provide insights into the role of osteopathy as a non-pharmacological approach in post-surgical care.
Who should consider this trial
Good fit: Ideal candidates are individuals who have had lumbar arthrodesis within the last four weeks and are experiencing postoperative mechanical pain.
Not a fit: Patients with neuropathic pain, fibromyalgia, or other significant somatic or neuropsychiatric conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance recovery strategies for patients after lumbar surgery, potentially reducing disability and improving quality of life.
How similar studies have performed: While the specific combination of physiotherapy and osteopathy is less commonly studied, similar approaches in postoperative care have shown promising results in improving patient outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Paris
- Clinique Bizet — Paris, France (RECRUITING)
Study contacts
- Study coordinator: Bouchra benkessou, PM
- Email: b.benkessou@hexagone-sante-paris.fr
- Phone: 0033140693525
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Chirurgical Intervention