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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04964804
Other study ID # M2016207
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2015
Est. completion date May 14, 2016

Study information

Verified date June 2021
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 14, 2016
Est. primary completion date May 14, 2015
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Patients who need lumbar nerve root block treatment Exclusion Criteria: 1. Tumor patients 2. Patients who have had lumbar spine surgery before

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
real-time ultrasound-CT fusion imaging
selective lumbar nerve root block puncture under real-time ultrasound-CT fusion imaging
ultrasound alone
selective lumbar nerve root block puncture under the guidance of ultrasound alone

Locations

Country Name City State
China Department of Ultrasound Diagnosis, Peking University Third Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary 1 month VAS pain score Patients undergo VAS pain score after the sonographer performs selective lumbar nerve root block puncture VAS pain scores were performed 1 month after surgery
Primary 3 month VAS pain score Patients undergo VAS pain score after the sonographer performs selective VAS pain scores were performed 3 month after surgery
Primary 6 month VAS pain score Patients undergo VAS pain score after the sonographer performs selective VAS pain scores were performed 6 month after surgery
Primary 12 month VAS pain score Patients undergo VAS pain score after the sonographer performs selective VAS pain scores were performed 12 month after surgery
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