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Evaluating Handheld Metal Detectors for Spinal Implant Detection

Detection of Modern Spinal Implants by Handheld Metal Detectors - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/08/072947
Enrollment
300
Registered
2024-08-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 100 consecutive patients undergoing cervical spine, dorsal and lumbar spine instrumenta-tion with implants will be recruited

Exclusion criteria

Exclusion criteria: Patients with prior history of spinal instrumentation. Patients with pacemakers or other implanted metallic hardware that can interfere with detection of spinal implant

Design outcomes

Primary

MeasureTime frame
Demographic profile and BMI Region of spine operated Metal used Number of levels Anterior or posterior surgery Number and type of implants Weight of implantsTimepoint: This is a single point study requiring no further follow up or clinic visits from the patient for the purpose of data collection

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactDr Bharat R Dave

Stavya Spine Hospital And Research Institute

brd_172@yahoo.com9825019913

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026