Effect of lumbar transforaminal epidural block with high volume injectate without steroids in patients with lumbar spinal stenosis: a randomized, controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009196

Enrollment

Registered

2024-02-22

Start date

2024-02-01

Completion date

Unknown

Last updated

2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Patients are divided into two groups by randomized control. The low-dose group is injected with a mixture of 1 ml of 1% lidocaine, 1 ml of contrast , and 1 ml of liquid Hyaluronidase, and the h

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients diagnosed with spinal stenosis and undergoing lumbar transforaminal epidural nerve block

Exclusion criteria

Exclusion criteria: Patients with a history of lumbar interforaminal epidural nerve block within 4 weeks before or after the procedure, patients taking oral steroids, cognitive dysfunction, taking anticoagulants, or patients and guardians who do not consent to the study.

Design outcomes

Primary

Measure	Time frame
pain score (VAS) the Roland-Morris disability questionnaire , Questionnaire for medical outcome short form health survery	—

Secondary

Measure	Time frame
pain score(VAS) during procedure and spread pattern of contrast	—

Countries

Korea, Republic of

Contacts

Public ContactWon-joong Kim

Ewha Womans University Medical Center

ickypoo@naver.com+82-2-2650-5391

Outcome results