Last reviewed · How we verify
NCT06827795
An Open, Parallel-group, Randomized, Medical Device Study to Assess the Usability and Performance of Surgify HaloTM in Spine Surgery Versus State-of-art (Rosen Burr)
NA trial testing A burr used in spine surgery in Spine Surgery in 30 participants. Currently enrolling.
15 December 2026
Quick facts
| Lead sponsor | Surgify Medical Oy |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 30 |
| Start date | 19 February 2026 |
| Primary completion | 15 December 2026 |
| Estimated completion | 31 December 2026 |
| Sites | 1 location across United States |
Drugs / interventions tested
- A burr used in spine surgery
Conditions studied
- Spine Surgery — all drugs for Spine Surgery →
Sponsor
Surgify Medical Oy
Who can join
Adults 21 to 85, any sex, with Spine Surgery. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this research study is to: test the usability and performance of the medical device Surgify Halo ™ in revision spine surgery test the level of "chattering " during the use of the device test the cutting performance of Surgify Halo™in comparison to the usual drill bit used in spine surgery ( Rosen burr). This medical device is available for its indications for shaping and removal of hard tissue and bone in neurosurgical, spinal, ENT, and general surgical procedures. The target is to enroll 30 participants in this study.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06827795
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Spine Surgery
Currently open trials in the same condition.
- NCT07344467 — Oral Melatonin Versus Oral Pregabalin on Postoperative Pain and Anxiety Following Spine Surgery · NA · recruiting
- NCT06975072 — Effect of Magnesium on Neuromonitoring · Phase 4 · recruiting
- NCT06785350 — Minimum Effective Dose of Incisional Local Infiltration Betamethasone for the Prevention of Pain After Spinal Surgery · NA · recruiting
- NCT06439953 — Irrisept Solution for Instrumented Spine Surgery · NA · recruiting
Other Surgify Medical Oy trials
Trials by the same sponsor.
- NCT05269836 — Use of Surgify Safety Burr in Hard Tissue Cutting, Head and Spine Area · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06827795 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Surgify Medical Oy
- Last refreshed: 18 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06827795.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing