Trials / Recruiting
RecruitingNCT05277818
Post-marketing Clinical Follow-up of the Medical Device DIVA®
Clinical Follow-up of the DIVA® Device in Lumbar Disc Herniation Surgery
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 822 (estimated)
- Sponsor
- SC Medica · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Observational, ambispective, longitudinal, comparative, open, multicentric study. The main objective is to compare the performance of care in patients operated with and without DIVA®.
Detailed description
The primary endpoint is the reoperation for any cause (excluding trauma) on the lumbar spine.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Surgery lumbar disc herniation | Surgery for a degenerative or traumatic mono-segmental lumbar disc herniation |
Timeline
- Start date
- 2022-09-07
- Primary completion
- 2027-03-15
- Completion
- 2027-03-15
- First posted
- 2022-03-14
- Last updated
- 2022-10-31
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT05277818. Inclusion in this directory is not an endorsement.