Clinical and Biomolecular Assessment for the Monitoring of Patients Undergoing Regenerative Medicine Treatments with Orthobiologics
Condition(s) studied
Investigational drug(s) / intervention(s)
PRP and related devices to abtain platelet concentrate from whole blood, medullary and adipose tissue and related devices: PRP and related devices to abtain platelet concentrate from whole blood, medullary and adipose tissue and related devices
Study summary
the aim is to improve the evaluation of the outcomes of regenerative medicine treatments performed in the regenerative medicine centers involved in the study.
patients who undergo regenerative medicine treatments present acute and chronic pathologies of the musculoskeletal system, of the stomatological system and of the integuments.
Objective pre, peri and post treatment evaluations are collected. A dedicated software collects the PROMs compiled by the patients, the objective clinical data and the biomolecular evaluations.
Eligibility
Primary outcome measure(s)
- Change in Visual Analog Scale — Change between baseline and 12 months
Pain will be measured with Visual Analog Scale (0-10, where 0 rapresents absence of pain and 10 the maximum pain possible) before and after treatment.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Istituto Clinico San Siro (satellite center) | Milan | Italia | Recruiting |
| IRCCS Ospedale Galeazzi-Sant'Ambrogio (coordinator) | Milan | Italy | Recruiting |
More I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio trials in Italy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04711551 on ClinicalTrials.gov ↗ ← All trials in Italy