Prospective Clinical Evaluation of BD Spinal Needles

Status Completed

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

Clinical Trial Details

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

View Details

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