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Clinical Trials/CTRI/2022/05/042811
CTRI/2022/05/042811CompletedPhase 4

A prospective, post market, non-interventional observational, open label, single arm, single center study to confirm the clinical safety and performance of Skanray’s Patient Monitors

Skanray Technologies Limited0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 4
Status
Completed

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Inclusion Criteria

  • Adult, pediatric and neonatal subjects of either genders.
  • The patients who need continuous physiological parameters monitoring in different areas of the hospital (Ex; ICU, OT, emergency, wards, operative care etc.)
  • The subjects or the legally authorised representative capable of understanding and signing the informed consent.

Exclusion Criteria

  • Subjects who are to be monitored in an MRI environment or in an oxygen-enriched environment.
  • Neonates shall be excluded for ST segment and arrhythmia analysis.

Investigators

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