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Effect of supraneural transforaminal epidural steroid injection combined with caudal epidural steroid injection with catheter in chronic radicular pain management:Double blinded randomized controlled trial

Effect of supraneural transforaminal epidural steroid injection combined with caudal epidural steroid injection with catheter in chronic radicular pain management:Double blinded randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20171101002
Enrollment
54
Registered
2017-11-01
Start date
2017-11-21
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic lumbosacral radicular pain Transforaminal &#44

Interventions

Supraneural transforaminal epidural steroid injection 40 mg of triamcinolone,Supraneural transforaminal epidural steroid injection 40 mg triamcinolone plus caudal epidural steroid injection with cathe
Transforaminal pidural steroid injection,Transforaminal epidural steroid injection plus caudal epidural steroid injection with catheter

Sponsors

Phramongkutklao Hospital.
Lead Sponsor
Phramongkutklao College of Medicine
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 18-80 years, who had a history of chronic lumbosacral radicular pain (longer than 6 months), unsatisfactory pain control with oral pharmacotherapy, physical therapy and no indication for surgery were enrolled in this study.

Exclusion criteria

Exclusion criteria: Patients who had significant neurological deficit or cauda equine syndrome, no absolute contraindication to intervention from MRI such as discitis or spinal infection, coagulopathy, history of allergy to local anesthetics, contrast media, triamcinolone, psychiatric problem, pregnancy and language barrier

Design outcomes

Primary

MeasureTime frame
Pain Score(Verbal numerical rating scale,VNRS) Before procedure at 1,3 and 6 month after procedure The effective response to procedure was defined by 30 point-reduction of VAS from baseline

Secondary

MeasureTime frame
Functional outcome Before procedure at 1,3 and 6 month after procedure Assessed by The Oswestry Low Back Pain Disability Questionnaire

Countries

Thailand

Contacts

Public ContactSithapan Munjupong

Phramongkutklao Hospital

sithapan@gmail.com+66841153691

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026