About this trial
The aim of the study is to determine the efficacy of an Amniotic Fluid Tissue Product for pain relief and functional improvements for all types of musculoskeletal conditions. The study is prospective, with outcome measures being obtained at numerous time points after the regenerative procedure.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age 18 and over.
Ability to attend follow up visits or at least converse on phone or complete email follow up forms.
Disqualifiers
Active Infection
Pregnancy, Lactating
Clotting disorder
Trial design
Single group
Treatments tested in this trial
Umbilical Allograft
Other interventionThe umbilical allograft is regulated by the FDA and comes from a lab that is FDA registered.
Treatment groups
Trial outcomes
Primary outcomes
Short Musculoskeletal Function Assessment Questionnaire (SMFA)
The Short Musculoskeletal Function Assessment Questionnaire (SMFA) is designed to measure the functional status of patients with a broad range of musculoskeletal injuries and disorders.
Secondary outcomes
Work Status
Not Working, Part Time, Full Time, Retired
Visual Analog Scale (VAS)
Assesses pain based on a scale from 0 to 100
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: