A Comparative Study of Erector Spinae Fascia (ESF) Injection and Dry Needling Combined With Functional Rehabilitation (FR) in Patients With Chronic Low Back Pain Who Have Undergone Spinal Surgery (SPIN-NEED)
- NCT ID
- NCT07555496
- Registry status
- Recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- Clinique de la Côte d'Emeraude
Overview
ClinicalTrials.gov lists this study as Recruiting.
Enrollment: 120 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Patient with chronic back pain, with previous surgery
Exclusion Criteria:
* Patients with specific or common low back pain
* Patients receiving posterior subcutaneous spinal cord stimulation
* Patients with a life expectancy of less than 12 months
* Patients with a contraindication to corticosteroid injections (coagulation disorder)
* Pregnant or breastfeeding patients
* Patients with cognitive and/or psychobehavioral disorders
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: France
Sample of listed locations
- Emerald Coast Clinic — St-Malo, 35400, France — Site recruitment status not specified in the registry data
Study details
- Start date
- September 7, 2026
- Primary completion date
- December 31, 2028
- First posted
- April 29, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07555496
- Registry last updated
- September 11, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07555496 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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