Diabetic Foot Ulcer Clinical Trials
2 recruiting trials for Diabetic Foot Ulcer. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Diabetic Foot Ulcer clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Applied Biologics, LLC (1), University of Minnesota (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is SLAM + SOC (other, 1 trial), followed by SOC, Total Contact Soft Cast.
Track Diabetic Foot Ulcer trials
Subscribe for TrialFinderData updates by email. No spam, unsubscribe anytime.
Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
Evaluating the Efficacy of a Single Layer Placental-based Allograft and Standard of Care Versus Standard of Care
A Randomized Controlled Multicenter Clinical Trial, Evaluating the Efficacy of a Single Layer Placental-based Allograft and Standard of Care versus Standard of Care alone in the...
Total Contact Soft Cast in Diabetic Foot Ulcers
To determine the effectiveness, compliance, patient tolerance, ease of use and safety of total contact soft cast in diabetic foot ulcers.
Explore Other Conditions
Frequently Asked Questions
There are currently 2 clinical trials for Diabetic Foot Ulcer, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Diabetic Foot Ulcer, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Diabetic Foot Ulcer, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.