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NCT04774029 · ClinicalTrials.gov registry record · Early Phase 1

Basivertebral Nerve Block During Vertebral Augmentation: An Alternative Approach to Intraprocedural Pain Management

A Early Phase 1 study of Vertebral Fracture and Vertebral Compression, sponsored by Northwell Health.

Completed
Registry status
Early Phase 1
Development phase
10
Enrollment target
1
Study location

NCT04774029 is a Early Phase 1 study of Vertebral Fracture and Vertebral Compression that has completed, run by Northwell Health. The registered enrollment target is 10 participants, below the 39-participant average among 3 other Vertebral Fracture trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04774029, a Early Phase 1 study of Vertebral Fracture and Vertebral Compression, has completed, sponsored by Northwell Health.

COMPLETED
Registry status
Early Phase 1
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

The goal of this study is to assess the efficacy of lidocaine basivertebral nerve block as intraprocedural anesthesia during vertebral augmentation procedures.

Interventions

  • PROCEDURE Basivertebral nerve block
  • DRUG Lidocaine induced basivertebral nerve block

Study Locations (1)

New York

  • Northwell Health Mather Hospital - Port Jefferson

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2020-01-10
Est. Completion 2020-05-01
Phase Early Phase 1

Sponsor

Northwell Health

370 total trials

What the Registry Record Tells You About NCT04774029

The ClinicalTrials.gov registry entry for NCT04774029 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 39-participant average among 3 other Vertebral Fracture trials with a reported enrollment target (74% lower). The listed sponsor is Northwell Health, which has 370 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Vertebral Fracture appearing as the primary indexed condition, and to 2 interventions - of which Basivertebral nerve block is the first listed.

NCT04774029 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT04774029 about?

NCT04774029 is a clinical study titled "Basivertebral Nerve Block During Vertebral Augmentation: An Alternative Approach to Intraprocedural Pain Management". The goal of this study is to assess the efficacy of lidocaine basivertebral nerve block as intraprocedural anesthesia during vertebral augmentation procedures.

What is the current status of trial NCT04774029?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 10 participants. The study started on 2020-01-10. Estimated completion is 2020-05-01.

What conditions does trial NCT04774029 study?

This clinical trial studies the following conditions: Vertebral Fracture, Vertebral Compression, Vertebra Compression Fracture.

What interventions are being tested in trial NCT04774029?

The interventions under investigation include: Basivertebral nerve block (PROCEDURE), Lidocaine induced basivertebral nerve block (DRUG).

Who is sponsoring clinical trial NCT04774029?

This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04774029 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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