Assessing the efficacy of Fibergraft Bioactive Glass in patients undergoing posterolateral lumbar fusion surgery
Not Applicable
- Conditions
- umbar degenerative disc diseaseLumbar degenerative disc diseaseSurgery - Other surgeryMusculoskeletal - Other muscular and skeletal disorders
- Registration Number
- ACTRN12624000320550
- Lead Sponsor
- SpinePlus
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 39
Inclusion Criteria
1. Age greater than or equal to 18 at the time of surgery
2. Scheduled to undergo a one or two level PLF with a single surgeon at a private surgical practice
Exclusion Criteria
1. Active workers compensation claim
2. Unable to participate in the required follow-up appointments
3. Ineligible to participate in the study as determined by the Principal Investigator
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method