Levagen+ Efficacy Study on Diabetic Peripheral Neuropathy

Recruiting Phase 2 Interventional Study
Diabetic Peripheral Neuropathy
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
80 (estimated)
Sponsor
RDC Clinical Pty Ltd · Industry
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About This Trial

The goal of this clinical trial is to assess the efficacy of Levagen+ supplementation for the symptoms of diabetic peripheral neuropathy (DPN) in patients with DPN. Participants will have remote visits and attend a local pathology centre for blood draws. They will take the study product for 12 weeks, from baseline to week 12 they will have remote visits every 3 weeks.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adults aged 18-75 years. * Using prescribed glucose-lowering medications, including oral medications (stable dose for 3 months or more) and/or insulin for diabetes (type 1 or 2). * Scoring12 or more on the Self-reported Leeds Assessment of Neuropathic Symptoms and Signs (S-LAN…
Contacts

Amanda Rao

+61(0)731024486

research@rdcglobal.com.au

CONTACT