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A Study Comparison of Clinical Outcome After Different Rate of Infusion in Caudal Epidural Steroid Injection

NCT02939482 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 112

Last updated 2019-06-25

No results posted yet for this study

Summary

The purpose of this study is to determine the effects of different rates of Caudal Epidural Steroid Injection (CESI) on clinical outcomes of the patients.

Conditions

  • Spinal Stenosis
  • Lumbosacral Spondylosis
  • Radiculopathy

Interventions

DRUG

Triamcinolone Acetonide and normal saline solution

80 mg/2 ml Triamcinolone Acetonide and 18 ml normal saline solution

Sponsors & Collaborators

  • Navamindradhiraj University

    lead OTHER

Principal Investigators

  • Satit Thiengwittayaporn, M.D. · Navamindradhiraj University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-01
Primary Completion
2018-08-02
Completion
2019-01-30

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02939482 on ClinicalTrials.gov