Result
Tissue integrity · Secondary, pre-specified · Efficacy
Effect as reported: [object Object]
Location in the source: [results]
SECONDARY · Number of Participants Stratified by Change From Baseline in Spinal Cord Anatomy - Spinal Cord Adhesion (Presence or Absence) · unit: Participants · measured at: 6 months post-implantation Neuro-Spinal Scaffold: 1
Study
NCT02138110/brief_summary
human Human · Open label · Uncontrolled · 72h – 14 days · Complete
Participants actually studied: 20
No dataNothing has been recorded here yet. This is not a zero.
What this result says about which claim
- Partially supports — Implantation of a bioresorbable polymer scaffold into the injured spinal cord is associated with serious adverse events.
SECONDARY · Number of Participants Stratified by Change From Baseline in Spinal Cord Anatomy - Spinal Cord Adhesion (Presence or Absence) · unit: Participants · measured at: 6 months post-implantation