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The Effect of Epidural Steroid Use in Patients With Continous Epidural Block in PHN Patients.

The Effect of Epidural Steroid Use on Pain Relief in Patients With Continuous Epidural Nerve Block in Postherpetic Neuralgia Patients.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03995563
Enrollment
40
Registered
2019-06-24
Start date
2019-05-15
Completion date
2020-11-30
Last updated
2019-06-24

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

Conditions

Neuralgia,Postherpetic

Brief summary

The efficiency of epidural steroid injection in patients who has postherpetic neuralgia is well known. In this study, the purpose is whether the continous epidural steroid injection is effective or not.

Detailed description

Continous epidural injection will be done during 10 days. D group will be injected a 0.19% ropivacaine 8mL and dexametasone 1mg every other day during 10 days. Continous epidural injection will be done during 10 days N group will be injected a 0.19% ropivacaine 8mL only every other day during 10 days

Interventions

DRUGDexamethasone

Continous epidural injection will be done during 10 days. D group will be injected a 0.19% ropivacaine 8mL and dexametasone 1mg every other day during 10 days. .

DRUGRopivacaine

Continous epidural injection will be done during 10 days Both group will be injected a 0.19% ropivacaine 8mL every other day during 10 days

Sponsors

Korea University Guro Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients who has herpes zoster * Patients has a period (at least 1month) after onset of herpes zoster * Patients has a definite symptom along dermatome * ASA class I - II * Age : 18 - 80 years

Exclusion criteria

* Patients who has a cancer * Patients who has a neurologic, psychologic, renal, hepatic and hematologic disease * Patients who has a other dermatologic disease * Patients who has major operation & procedure history * Patients who has a other pain origin * Patients who can not be inserted epidural catheter

Design outcomes

Primary

MeasureTime frameDescription
VAS scoreup to 10 daysThe investigator set the primary outcome If there is a 50% reduction of VAS score.

Countries

South Korea

Contacts

Primary ContactJung Eun Kim, MD, PhD
geri200@gmail.com+82-10-7271-5391

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026