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Clinical Trial Summary

Post-market, observational study to assess the real-world safety and efficacy of BD Spinal Needles used in an on-market fashion.

Clinical Trial Description

Single-arm, post-market, observational, prospective study of participants who will receive neuraxial procedures with a BD Spinal Needle as part of their routine medical care. Patients will be followed from BD Spinal needle insertion up to 7 days after the insertion according to the routine medical care and site policy. Data collected will be gathered from the patient's medical charts. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05214560
Study type Observational
Source Becton, Dickinson and Company
Status Completed
Start date February 10, 2022
Completion date July 22, 2022

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