Comparing wound closure techniques in spine surgery
Assessment of Wound Closure Techniques in Primary Spine Surgery Using SPY Intra-operative Angiography
NA · Mayo Clinic · NCT04396613
This study tests which of three different ways to close wounds after spine surgery helps adults with spinal stenosis heal better.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 147 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Mayo Clinic (other) |
| Locations | 1 site (Rochester, Minnesota) |
| Trial ID | NCT04396613 on ClinicalTrials.gov |
What this trial studies
This study investigates the differences in blood flow around wound sites when using three different wound closure techniques in patients undergoing primary spine surgery. The researchers aim to determine which technique may promote better healing and outcomes. Eligible participants include adults with spinal stenosis who require surgical intervention for decompression or fusion. The study will assess the effectiveness of these techniques in a controlled surgical setting.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with a primary diagnosis of spinal stenosis requiring surgical intervention.
Not a fit: Patients with previous spinal surgery, systemic corticosteroid use, or certain chronic conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved healing and recovery outcomes for patients undergoing spine surgery.
How similar studies have performed: Other studies have explored various wound closure techniques, but this specific comparison in the context of spine surgery is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥ 18 years old * Primary diagnosis of spinal stenosis * Surgical indication for 1 or 2 level posterior spinal decompression or fusion Exclusion Criteria: * Pregnant or Breastfeeding * Previous posterior spinal surgery * Systemic corticosteroid use * Long-term anticoagulation treatment * Diagnosis of diabetes mellitus * Diagnosis of peripheral arterial disease * Current smoker * Active infection of any kind or chronic infection with HIV, Hepatitis C, or Syphilis * Iodine Allergy
Where this trial is running
Rochester, Minnesota
- Mayo Clinic — Rochester, Minnesota, United States (RECRUITING)
Study contacts
- Principal investigator: Arjun Sebastian — Mayo Clinic
- Study coordinator: Cassandra Willson
- Email: Kingsbury.Cassandra@mayo.edu
- Phone: 507-293-4290
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Spinal Injuries