Syringe Pressure Analysis: A Critical Examination of the Operator's Burden

NCT06476353 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 224

Last updated 2024-06-27

No results posted yet for this study

Summary

This was a randomized prospective clinical trial conducted from October 1, 2023, to May 15, 2024, at the University Surgery Center in Merced, CA. The project was approved by the MetroWest Medical Center Institutional Review Board (IRB). Patients in each procedure group were categorized into groups and randomly distributed into four sub-groups based on the syringe size used (5ml, 10ml, 20ml, 30ml). A medical grade force sensor device was used to collect the necessary real-time syringe force data. An analysis of variance (ANOVA), and pairwise t test were used to make comparisons between means and determine statistical significance.

Conditions

  • Back Pain Lower Back Chronic

Interventions

OTHER

Analysis of Force and Pressure Requirements across Syringe Sizes for Pain Management Procedures

The investigators are analyzing the compression force required to plunge different syringe sizes to determine the operator's burden.

Sponsors & Collaborators

  • Orthospine Advance Health, Inc.

    lead OTHER

Principal Investigators

  • Gabriel Garcia-Diaz, MD · Orthospine Advance Health

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-01
Primary Completion
2024-05-15
Completion
2024-05-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06476353 on ClinicalTrials.gov