Clinical Trials Directory

Trials / Completed

CompletedNCT04108507

Prevention of Residual Low Back Pain After Percutaneous Kyphosis(PKP) Using Posterior Branch Block of Spinal Nerve

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
198 (actual)
Sponsor
Second Affiliated Hospital of Wenzhou Medical University · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to block the posterior branch of lumbar spinal nerve during PKP operation and compare it with the patients without spinal nerve block, so as to verify the effect of posterior branch block of spinal nerve in relieving short-term and long-term residual low back pain after operation.

Detailed description

Patients older than 60 years old who underwent Percutaneous kyphosis(PKP) surgery for osteoporotic fractures were randomly divided into two groups. The lumbar spinal nerve branch was blocked with betamethasone and ropivacaine in the experimental group during PKP operation, while the lumbar spinal nerve branch block was not performed in the control group during PKP operation. The low back pain was evaluated at 1 week, 2 weeks, 1 month, 3 months and 6 months after operation using Visual analogue pain score(VAS)scale.So as to compare the effect of lumbar spinal nerve block on residual pain after PKP.

Conditions

Interventions

TypeNameDescription
PROCEDUREposterior branch block of spinal nerveposterior branch block of spinal nerve during Percutaneous kyphoplasty(PKP) operation

Timeline

Start date
2019-09-01
Primary completion
2020-10-24
Completion
2020-10-24
First posted
2019-09-30
Last updated
2020-10-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04108507. Inclusion in this directory is not an endorsement.