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Completed

NCT Number: NCT04964804

Comparative Study of Real-time Ultrasound-CT Fusion Imaging and Ultrasound-guided Selective Lumbar Nerve Root Block

The study is aimed at patients with low back and leg pain. The experimental group of patients underwent selective lumbar nerve root block puncture under real-time ultrasound-CT fusion imaging by sonographers, and the control group underwent puncture under the guidance of ultrasound alone by sonographers.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Ultrasound Diagnosis, Peking University Third Hospital

Beijing, Beijing Municipality, 100191, China

About this study

A total of 60 patients with low back and leg pain were randomly divided into two groups, 30 people in each group. Patients in the experimental group underwent selective lumbar nerve root block puncture under the real-time ultrasound-CT fusion imaging of the sonographer, and the control group underwent puncture under the sole ultrasound guidance of the sonographer. This study was used to compare the difference between the effects of pure ultrasound guidance and ultrasound-CT fusion imaging guidance on selective lumbar nerve root block.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients who need lumbar nerve root block treatment

Exclusion criteria

  • Tumor patients
  • Patients who have had lumbar spine surgery before

Treatment and study plan

real-time ultrasound-CT fusion imaging

Procedure

selective lumbar nerve root block puncture under real-time ultrasound-CT fusion imaging

ultrasound alone

Procedure

selective lumbar nerve root block puncture under the guidance of ultrasound alone

Primary outcomes

  1. 1 month VAS pain score

    Time frame: VAS pain scores were performed 1 month after surgery

    Patients undergo VAS pain score after the sonographer performs selective lumbar nerve root block puncture

  2. 3 month VAS pain score

    Time frame: VAS pain scores were performed 3 month after surgery

    Patients undergo VAS pain score after the sonographer performs selective

  3. 6 month VAS pain score

    Time frame: VAS pain scores were performed 6 month after surgery

    Patients undergo VAS pain score after the sonographer performs selective

  4. 12 month VAS pain score

    Time frame: VAS pain scores were performed 12 month after surgery

    Patients undergo VAS pain score after the sonographer performs selective

Sponsors and collaborators

Lead sponsor

Peking University Third Hospital

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2016
First posted
Jul 16, 2021
Registry last updated
Jul 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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