chronic refractory pain
Conditions
Interventions
All patients are investigated whether differences in the locations of adhesiolysis contributed to the outcomes of pain relief.In accordance with the findings of the fluoroscopic imaging, the patients
Sponsors
Oita University Faculty of Medicine, Department of Anesthesiology and Intensive Care Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients in whom the symptoms could not be sufficiently improved by conservative therapies, such as nerve blockade, oral medications with non-steroidal anti-inflammatory drugs or physical therapy, and patients in whom the symptoms could not be sufficiently imptover by surgical therapy. In all patients, fluoroscopic imaging using a contrast medium(10ml;OMNIPAQUE240) are performed to assess the condition of adhesion.All patients have adhesions in the locations of attributed to the pain.
Exclusion criteria
Exclusion criteria: Patients with hemorrhagic tendencies, psychiatric abnormalities or malignant diseases or severe liver disease or severe renal disease or drug allergy were also excluded from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual analogue scale(VAS),The Roland-Morris Disability Questionnaire,The Oswestry Disability Index 2.0,Japanese Orthopedic Association back pain treatment results evaluation criteria | — |
Countries
Japan
Contacts
Public ContactJunji Taktani
Oita University Faculty of Medicine Department of Anesthesiology and Intensive Care Medicine
Outcome results
None listed