Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06827795 · ClinicalTrials.gov registry record · NA
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)
A NA study of Spine Surgery, sponsored by Surgify Medical Oy.
- Recruiting
- Registry status
- NA
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT06827795: Recruiting NA study of Spine Surgery, sponsored by Surgify Medical Oy.
NCT06827795 is a NA study of Spine Surgery that is actively recruiting participants, run by Surgify Medical Oy. The registered enrollment target is 30 participants, below the 283-participant average among 6 other Spine Surgery trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06827795, a NA study of Spine Surgery, is actively recruiting participants, sponsored by Surgify Medical Oy.
- RECRUITING
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Primary Outcome
Test the level of "chattering " during the use of the device and test the cutting performance of Surgify Halo™ in comparison to the usual drill bit used in spine surgery ( Rosen burr)
Conditions Studied
Interventions
- DEVICE A burr used in spine surgery
Study Locations (1)
New York
- North Shore University Hospital - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2026-02-19 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
What NCT06827795 shows while recruiting
NCT06827795 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 283-participant average among 6 other Spine Surgery trials with a reported enrollment target (89% lower).
The record links to 1 condition, with Spine Surgery appearing as the primary indexed condition, and to 1 intervention - of which A burr used in spine surgery is the first listed.
NCT06827795 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06827795 about?
NCT06827795 is a clinical study titled "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)". 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 su...
What is the current status of trial NCT06827795?
This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2026-02-19. Estimated completion is 2026-12-31.
What conditions does trial NCT06827795 study?
This clinical trial studies the following conditions: Spine Surgery.
What interventions are being tested in trial NCT06827795?
The interventions under investigation include: A burr used in spine surgery (DEVICE).
Who is sponsoring clinical trial NCT06827795?
This trial is sponsored by Surgify Medical Oy, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06827795 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Spine Surgery
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Irrisept Solution for Instrumented Spine Surgery
RECRUITING · NA
-
Perioperative Intravenous Lidocaine or Epidural Anesthesia on Outcomes in Complex Spine Surgery
COMPLETED · NA
-
Influence of Dexmedetomidine on the Evoked Potentials During Spine Surgery
COMPLETED · NA
-
Evaluation of Open-Label Conditioned Placebo Analgesia for Postoperative Opioid Reduction Following Spinal Fusion
COMPLETED · NA
-
Effect of Magnesium on Neuromonitoring
RECRUITING · Phase 4
-
Intravenous Methocarbamol for Acute Pain After Spine Surgery
COMPLETED
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00977977 · 30 participants · Phase 2
Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy
- NCT01459107 · 30 participants · Phase 2
Human Upper Extremity Allotransplantation
- NCT01666080 · 30 participants · NA
Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)
- NCT01720836 · 30 participants · Phase 1
Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI