Evaluating the Efficacy of NeoThelium FT in the Treatment of Chronic Open Wounds
ConditionOpen Wound
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNuScience Medical Biologics, LLC
About this trial
This is a randomized controlled crossover trial evaluating the efficacy of NeoThelium FT in conjunction with standard of care vs. standard of care alone in treating chronic open wounds.
Eligibility criteria
Qualifiers
Male or Female, 18 years of age or older
Subject has a medical diagnosis of "other" Open wound
Subject has a chronic open wound present for 4 weeks or greater (documented in medical record), and less than 12 months duration if being treated with continuous SOC
Subject has a chronic open wound with a historical wound measurement showing less than 25% healing within 14 days prior to screening
Disqualifiers
Subject with a wound diagnosis of diabetic foot wound, pressure wound, venous leg wound, burn wound, or alternative diagnosis other than "open wound"
Subject has a known life expectancy of <1 year
Subject is unable to comply with protocol treatment
Subject has major uncontrolled medical disorders in the opinion of the investigator, such as serious cardiovascular, renal, liver, pulmonary, autoimmune, palliative care, or inherited blood disorders that may affect wound healing.
Trial design
Treatments tested in this trial
- Standard of Care
- NeoThelium FT
Treatment groups
132 Participants
are divided into 2 treatment groupsSponsors and collaborators
NuScience Medical Biologics, LLC
Lead sponsor
SygNola, LLC
Collaborator
Source ClinicalTrials.gov