Radicular pain, Spine. Spondylosis
Conditions
Interventions
Intervention 1: Intervention group: In the case group, 1 microgram of Dexmedetomidine per kilogram is administered along with Depomedrol. Depomedrol is administered as 40 mg for each facial foraminal
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients older than 20 years of age Failure of previous symptomatic treatment such as exercise, physiotherapy, and oral analgesics Patient consent to participate in the study
Exclusion criteria
Exclusion criteria: Patients with progressive weakness and muscle weakness Allergy to steroids Coagulopathy Steroid injection in the past 12 weeks Systemic infection Injection site infection Unstable mental and clinical condition Patients with spondylolisthesis Patient unwillingness to participate in the study Having a body mass index greater than 30 Patients with Cancer Patients with cardiovascular diseases Patients with hypertension
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Oswestry Disability. Timepoint: Before, one month, two months, and three months post intervention. Method of measurement: The Oswestry Disability Index (ODI).;Pain intensity. Timepoint: Before, one month, two months, and three months post intervention. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient Satisfaction. Timepoint: Before, one month, two months, and three months post intervention. Method of measurement: Patient Satisfaction Index (PSI). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactPooyan Alizadeh
Ahvaz University of Medical Sciences
Outcome results
None listed