Skip to content

A study on postoperative pain reduction through facet block after OLIF(Oblique lumbar interbody fusion) surgery

A study on postoperative pain reduction through facet block after OLIF(Oblique lumbar interbody fusion) surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007839
Enrollment
40
Registered
2022-10-25
Start date
2022-09-30
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

None listed

Interventions

Procedure/Surgery : A facet joint block in which drugs are administered directly to the lumbar facet joint that had undergone 1 level OLIF was performed immediately after surgery. At this time, 20mg o

Sponsors

Kyungpook National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) 20 years of age or older 2) Due to one of the following degenerative lumbar diseases Those who require oblique lateral lumbar interbody fusion in L3-4 or L4-5 single segment ? Spinal stenosis ? herniated disc ? Spondylolisthesis or spondylolysis 3) Adhere to treatment and procedures and observe all Those who are willing to visit the hospital for evaluation 4) A person who voluntarily signed a written consent after hearing the explanation about the purpose and method of this observational study

Exclusion criteria

Exclusion criteria: 1) Patients with severe osteoporosis (e.g., on DEXA bone density test, the mean T-score of lumbar L1-L4 < -4.0, or for young women, Z-score < -3.0 osteoporosis factor) 2) fracture of the application site (osteoporotic vertebral fracture, spine trauma fracture), subjects with acute infection, patients with the hemorrhagic disease, and patients with osteogenic disorders 3) Those with a history of fusion at the site of application 4) Those with a history of malignant tumors (the disease has been cured and Enrollment is possible if there has been no recurrence within 5 years) 5) Pregnant, lactating, or pregnant during this clinical trial You are planning or do not agree to a medically accepted method of contraception. those who do not 7) After being diagnosed with any of the following diseases, the operation proceeded. those who are judged to be difficult ? Uncontrolled diabetes, high blood pressure ? Mental illness: When it is difficult to conduct or comply with a clinical trial ? Drug and alcohol addiction ? Liver disease: liver cancer, cirrhosis, acute/chronic hepatitis ? Kidney disease: acute/chronic renal failure, excretory dysfunction ? Heart disease: severe heart failure ? Respiratory disease: active tuberculosis ? Infectious disease: active systemic infection and application site infection ? Metabolic diseases: rickets, osteomalacia, Paget's disease, pituitary dysfunction, (para)thyroid dysfunction, other bone metabolic disorders 8) It is difficult to conduct this observational study due to the judgment of the principal investigator patients who are considered to be

Design outcomes

Primary

MeasureTime frame
Visual analog scale for back pain

Secondary

MeasureTime frame
Adverse reactions

Countries

Korea, Republic of

Contacts

Public ContactSang-Woo Lee

Kyungpook National University Hospital

overload03@naver.com+82-53-200-5648

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026