Actively Recruiting
Relief of Lumbar Spinal Stenosis Symptoms
Led by Diskapi Teaching and Research Hospital · Updated on 2024-07-22
50
Participants Needed
2
Research Sites
22 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study was to compare the efficacy of caudal epidural steroid injection and caudal epidural pulsed radiofrequency stimulation in the relief of symptoms of lumbar spinal stenosis. This evaluation used the numerical rating scale (NRS) to assess pain relief and the Medication Quantification Scale III (MQS III) to assess the effectiveness of the interventions on medication consumption. The rates of adverse events related to the interventions were also compared.
CONDITIONS
Official Title
Relief of Lumbar Spinal Stenosis Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with lumbar spinal stenosis and spinal canal narrowing confirmed by examination and imaging
- Back and leg pain persisting for at least 3 months
You will not qualify if you...
- Previous lumbar surgery
- Pregnancy
- History of ongoing malignant disease
- Autoimmune diseases
- Active infection at the injection site
- Hematologic disorders
- Use of antiplatelet drugs
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Damla Yürük
Ankara, Türkiye, Turkey (Türkiye), 5319932
Actively Recruiting
2
Ankara Etlik City Hospital
Ankara, Yenimahalle, Turkey (Türkiye), 5319932
Actively Recruiting
Research Team
D
Damla T Yürük, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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