Failed back surgery syndrome. Other reaction to spinal and lumbar puncture
Conditions
Interventions
Intervention 1: Intervention group: Intervention group I, patients in the foraminal group will first receive Omnipaque 240 contrast agent, followed by 0.2% bupivacaine. Next, a combination of 150 unit
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who have a history of pain for at least three months, with or without radicular pain, following spinal surgery despite adequate medication Age over 18 years Having epidural adhesions based on clinical findings and MRI imaging
Exclusion criteria
Exclusion criteria: Pregnant and breastfeeding women Having suspected facet joint pain Receipt of any epidural injection or other invasive treatment methods within the past six months Substance addiction Having mental health issues
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The rate of pain. Timepoint: Before the intervention and at 4 and 12 weeks after intervention. Method of measurement: Visual Analogue Scale (VAS).;Functional status. Timepoint: Before the intervention and at 4 and 12 weeks after intervention. Method of measurement: Oswestry Disability Index questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Sharafi
Mashhad University of Medical Sciences
Outcome results
None listed