postoperative intrathecal analgesia for lumber spine surgery
- Conditions
- Musculoskeletal DiseasesSurgery
- Registration Number
- PACTR202304865602085
- Lead Sponsor
- Dr. Mona Raafat Elghamry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 88
both sex
ASA physical status I &II
age range 30-60 years old
scheduled to undergo elective open posterior lumbar interbody fusion surgery at 1 or 2 level
•Body mass index >35 kg/m2.
•Patients with neurological deficit (symptoms of lumbar intervertebral nerve injury (determined by a neurosurgical specialist based on physical and imaging examinations).
•Redo or previous lumber surgery.
•Allergy or contraindication to the given study drugs.
•Patients on chronic pain medication.
•Chronic alcoholism, history of a major psychiatric disorder or cognitive disorder (inability to understand the VAS).
•Any contraindication to intrathecal injection.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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