Health Condition 1: null- Lumbar Disc Diseases
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients are included in the study if all of the following criteria are met: 1.Patients having single level disc disease (L4/5 or L5 S1): Degenerative/ Disc prolapse 2.Patients having Supine lying pain (LBP/ leg pain/ discomfort/ numbness). 3.Psychosocially, mentally and physically able to fully comply with this protocol including adhering to scheduled visits, treatment plan, completing forms, and other study procedures; 4.Personally signed and dated informed consent document prior to any study-related procedures indicating that the patient has been informed of all pertinent aspects of the study. 5.Male or Female,having age between 35-70 yrs
Exclusion criteria
Exclusion criteria: Patients are excluded from participating in this study if any of the following criteria are met: 1.Has had previous surgery at the index level; 2.Has a fused level adjacent to the index level; 3.Patients with Diffused Idiopathic Skeletal Hyperostosis (DISH); 4.Active systemic or local infection; 5.Known or documented history of communicable disease, including AIDS or HIV; 6.Active hepatitis (receiving medical treatment within two years); 7.Active rheumatoid arthritis, non-controlled diabetes mellitus. 8.Immunologically suppressed, history of Pagetââ?¬•s disease, osteomalacia, or any other metabolic bone disease; 9.Morbid obesity defined as a body mass index > 40 kg/m2 or weight more than 100 pounds over ideal body weight; 10.Active malignancy. A patient with a history of any invasive malignancy (except non-melanoma skin cancer), unless treated with curative intent and there has been no clinical signs or symptoms of the malignancy for more than 5 years; 11.Current or recent history (within last 2 years) of substance abuse (e.g., recreational drugs, narcotics, or alcohol); 12.Pregnant or planning to become pregnant during study period; 13.Patients who are incarcerated. 14.Patients who have limited life expectancy due to significant medical comorbidities.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Association of supine lying low back pain/leg pain with retrolisthesisTimepoint: 1st Day Assessment | — |
Secondary
| Measure | Time frame |
|---|---|
| NilTimepoint: Nil | — |
Countries
India
Contacts
Stavya Spine Hospital and Research Institute