Epidural Dexamethasone Versus Betamethasone for Treatment of Lumbosacral Radiculalgia
- Registration Number
- NCT02833116
- Lead Sponsor
- Basque Health Service
- Brief Summary
This study evaluate the administration of epidural betamethasone versus dexamethasone for pain reduction, consumption of analgesic and quality of life. Half of the patient will receive dexametasone and the other half betametasone.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 320
Inclusion Criteria
- Unilateral leg pain secondary to lateral stenosis, disc protrusion or herniated disc.
- Age between 18 and 80 years.
- Moderate to severe pain (NVS>4).
- Right proficient oral and written language.
Exclusion Criteria
- Patients with high intracranial pressure.
- Patients with Multiple Sclerosis.
- Patients with Guillain-Barré syndrome radiculopathy of vascular origin.
- Patients with previous lumbar surgery.
- Patients pregnant or lactating.
- Patients with allergy or intolerance to any of the drugs used.
- Patients with severe cognitive impairment.
- Patients with intrathecal injectio radiculalgia.
- Patients with poorly controlled major psychiatric pathology.
- Patients with type I diabetes or poorly controlled type II diabetes (Hb1Ac>8.5).
- Patients with glaucoma.
- Patients with caudal equine syndrome.
- Patients with pre-treatment with steroid injections/or local anesthetics.
- Patients with central canal stenosis.
- patients with chronic treatment with oral corticosteroids without stabilized pattern.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group Betamethasone Betamethasone One ampule containing 12 mg of betamethasone in a syringe of 10 ml Group Dexamethasone Dexamethasone One ampule containing 4 mg of dexamethasone in a syringe os 10 ml
- Primary Outcome Measures
Name Time Method Pain. 3 months. Pain according to numerical visual pain scale.
- Secondary Outcome Measures
Name Time Method Quality of life. 7 days, 1, 3 and 6 months. Quality of life according to SF-36.
Pain. 7 days, 1, 3 and 6 months. Pain according to numerical visual pain scale.
Adverse events. 7 days, 1, 3 and 6 months. Adverse events.
Trial Locations
- Locations (1)
Enrique Barez
🇪🇸Vitoria-Gasteiz, Álava, Spain