MedPath

Comparison of caudal epidural method with S1 transforaminal block in patients undergoing lumbar discectomy

Phase 2
Recruiting
Conditions
Pain.
Other chronic pain
G89.29
Registration Number
IRCT20190325043107N31
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
52
Inclusion Criteria

Patients who underwent lumbar discectomy and have lower radicular pain symptoms.
Consent to participate in the research project

Exclusion Criteria

Taking anticoagulant drugs
Systemic infection
History of severe heart disease
Lumbar infection

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before the intervention, one month and three months after the intervention. Method of measurement: Visual Analog Scale (VAS).
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath