Clinical trial

Prediction Of Transforaminal Epidural Injection Success in Sciatica

Name
POTEISS
Description
Rationale: Treatment with transforaminal epidural injections is part of usual care in patients suffering from lumbar radiculopathy. However, not all patients experience a satisfactory result from this treatment and it is unclear what percentage of patients responds well and if any clinical or radiological factors exist that predict a positive response. Objectives: Primary: to develop a model based on demographic, clinical and radiological parameters for prediction of treatment success after TEI Secondary: to estimate the short-term efficacy of TEI in patients with LDH and spinal stenosis based on pain, functionality and perceived recovery scores, to determine the correlation between clinical and radiological baseline parameters and physical and psychological patient outcome measures, to determine the rate of additional injections and rate of surgery after treatment with TEI, to determine the short-term (cost)effectiveness of TEI on physical and psychological patient outcome measures, and to determine the rate of complications associated with TEI Study design: Prospective cohort study Study population: Patients that are scheduled for TEI as part of usual care suffering from a new episode of lumbar radiculopathy Main study parameters/endpoints: leg and back pain scores at baseline, 30 minutes, 2 and 6 weeks after treatment. ODI, HADS, Quality of Life and PCI at baseline, 2 and 6 weeks after treatment. Perceived recovery at 2 and 6 weeks after treatment. Usage of healthcare at baseline, 2 and 6 weeks after treatment.
Trial arms
Trial start
2020-11-15
Estimated PCD
2026-12-01
Trial end
2026-12-01
Status
Recruiting
Treatment
Transforaminal Epidural Injection
Injections above L3 will contain 1,5 ml lidocaine 1% and 10 mg dexamethasone and injections at L3 or below will contain 1,5 ml lidocaine 2% and 40mg methylprednisolone acetate in accordance with current Dutch anesthesiologic guidelines for usual care.
Arms:
Patients with Lumbar Disc Herniation, Patients with Lumbar Spinal Stenosis
Other names:
Transforaminal Epidural Steroid Injection
Size
388
Primary endpoint
Numerical Rating Scale Leg Pain
2 weeks
Eligibility criteria
Inclusion Criteria: * Diagnosis of unilateral lumbar radiculopathy secondary to LDH or one-level spinal stenosis * Diagnosis supported by magnetic resonance imaging (MRI) findings * Scheduled appointment for TEI * Access to e-mail * Signed informed consent Exclusion Criteria: * Diagnosis of unilateral lumbar radiculopathy secondary to LDH or one-level spinal stenosis * Age under 18 years * Severe multisegmental spinal disease * Anatomical abnormalities that may complicate the procedure technically (e.g. severe scoliosis) * Active malignancy or infectious disease * Use of immunosuppressive drugs * Use of systemic corticosteroids in preceding 3 months * Previous treatment with TEI for current episode of lumbar radiculopathy * History of lower back surgery at the same lumbar level * Circumstances that prevent treatment with TEI (e.g. use of anticoagulants that cannot be temporarily discontinued, allergy against steroids or local anaesthetic) * Pregnancy * Major language barrier
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'PROSPECTIVE'}, 'enrollmentInfo': {'count': 388, 'type': 'ESTIMATED'}}
Updated at
2023-10-12

1 organization

1 product

3 indications

Organization
Eja Verheijen
Indication
Sciatica
Indication
Herniated Disc