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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03995563
Other study ID # 2019-04-011
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date May 15, 2019
Est. completion date November 30, 2020

Study information

Verified date June 2019
Source Korea University Guro Hospital
Contact Jung Eun Kim, MD, PhD
Phone +82-10-7271-5391
Email geri200@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date November 30, 2020
Est. primary completion date May 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexamethasone
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. .
Ropivacaine
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

Locations

Country Name City State
Korea, Republic of Kangnam sacred heart hospital Seoul Yeongdeungpo-gu

Sponsors (1)

Lead Sponsor Collaborator
Korea University Guro Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary VAS score The investigator set the primary outcome If there is a 50% reduction of VAS score. up to 10 days
See also
  Status Clinical Trial Phase
Completed NCT00636636 - Safety and Efficacy of Gabapentin in Postherpetic Neuralgia Phase 3
Completed NCT04488835 - Pulsed Electromagnetic Field Therapy Versus Transcutaneous Electrical Nerve Stimulation in on Post-herpetic Neuralgia of the Sciatic Nerve N/A