Project Details
Project Description
A prospective, randomised, placebo-controlled, safety and feasibility trial to assess the effects of intravenous denosumab on bone mass in post-menopausal female intensive care patients expected to require greater than 24 hours of mechanical ventilation.
| Short title | Skeletal Outcomes Following Intensive Care |
|---|---|
| Acronym | SOFTER |
| Status | Not started |